UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
MyVariant Identifiers:
chr10:g.90774033T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.89014276T>A , CM000672.2:g.89014276T>A | GRCh38 |
| NC_000010.10:g.90774033T>A , CM000672.1:g.90774033T>A | GRCh37 |
| NC_000010.9:g.90764013T>A | NCBI36 |
| NG_009089.2:g.28746T>A , LRG_134:g.28746T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313771.10:n.1143T>A | ||
| ENST00000355740.8:c.*157T>A | ENSP00000347979.3:n.*157T>A | |
| ENST00000357339.7:c.771T>A | ENSP00000349896.2:p.Leu257= | |
| ENST00000371857.8:n.2379T>A | ||
| ENST00000460510.6:c.117T>A | ENSP00000512812.1:p.Leu39= | |
| ENST00000466081.6:n.2483T>A | ||
| ENST00000477270.6:c.879T>A | ENSP00000512813.1:p.Leu293= | |
| ENST00000479522.6:c.*263T>A | ENSP00000424113.1:n.*263T>A | |
| ENST00000484444.6:c.*275T>A | ENSP00000420975.1:n.*275T>A | |
| ENST00000488877.6:c.725T>A | ENSP00000425159.1:n.725T>A | |
| ENST00000492756.7:c.*263T>A | ENSP00000422453.1:n.*263T>A | |
| ENST00000494799.6:c.117T>A | ENSP00000512834.1:p.Leu39= | |
| ENST00000562983.3:c.117T>A | ENSP00000512845.1:p.Leu39= | |
| ENST00000612663.6:c.*236T>A | ENSP00000477997.3:n.*236T>A | |
| ENST00000640140.2:n.979T>A | ||
| ENST00000640250.2:n.333T>A | ||
| ENST00000640681.2:n.938T>A | ||
| ENST00000696723.1:n.4467T>A | ||
| ENST00000696741.1:n.2472T>A | ||
| ENST00000696742.1:n.2199T>A | ||
| ENST00000696743.1:n.3602T>A | ||
| ENST00000696744.1:n.873T>A | ||
| ENST00000696767.1:n.1168T>A | ||
| ENST00000696768.1:c.*157T>A | ENSP00000512859.1:n.*157T>A | |
| ENST00000696769.1:n.2523T>A | ||
| ENST00000696771.1:c.117T>A | ENSP00000512860.1:p.Leu39= | |
| ENST00000696772.1:n.2437T>A | ||
| ENST00000696773.1:n.2176T>A | ||
| ENST00000696774.1:n.5944T>A | ||
| ENST00000696776.1:c.927T>A | ENSP00000512861.1:p.Leu309= | |
| ENST00000696777.1:n.2242T>A | ||
| ENST00000696778.1:n.1270T>A | ||
| ENST00000696779.1:c.441T>A | ENSP00000512862.1:p.Leu147= | |
| ENST00000696780.1:c.864T>A | ENSP00000512863.1:p.Leu288= | |
| ENST00000696781.1:c.579T>A | ENSP00000512864.1:p.Leu193= | |
| ENST00000696782.1:c.*236T>A | ENSP00000512865.1:n.*236T>A | |
| ENST00000696783.1:n.2702T>A | ||
| ENST00000696992.1:n.1951T>A | ||
| ENST00000696995.1:n.4363T>A | ||
| ENST00000696996.1:n.2276T>A | ||
| ENST00000696997.1:c.*464T>A | ENSP00000513028.1:n.*464T>A | |
| ENST00000696998.1:n.2088T>A | ||
| ENST00000696999.1:c.117T>A | ENSP00000513029.1:p.Leu39= | |
| ENST00000697035.1:c.*167T>A | ENSP00000513059.1:n.*167T>A | |
| ENST00000697036.1:c.*250T>A | ENSP00000513060.1:n.*250T>A | |
| ENST00000697037.1:n.869T>A | ||
| ENST00000697093.1:n.3070T>A | ||
| ENST00000697094.1:n.3417T>A | ||
| ENST00000697095.1:c.*2035T>A | ENSP00000513104.1:n.*2035T>A | |
| ENST00000697096.1:n.1967T>A | ||
| ENST00000697097.1:c.117T>A | ENSP00000513105.1:p.Leu39= | |
| ENST00000562983.2:n.1020T>A | ||
| ENST00000690268.1:c.915T>A | ENSP00000509810.1:p.Leu305= | |
| ENST00000355740.7:c.*160T>A | ENSP00000347979.3:n.*160T>A | |
| ENST00000612663.5:c.*236T>A | ENSP00000477997.3:n.*236T>A | |
| ENST00000640140.1:n.1006T>A | ||
| ENST00000640250.1:n.333T>A | ||
| ENST00000640681.1:n.955T>A | ||
| ENST00000652046.1:c.834T>A MANE Select | ENSP00000498466.1:p.Leu278= | |
| ENST00000352159.8:c.*151T>A | ENSP00000345601.4:n.*151T>A | |
| ENST00000355279.2:c.809T>A | ENSP00000347426.2:n.809T>A | |
| ENST00000355740.6:c.834T>A | ENSP00000347979.2:p.Leu278= | |
| ENST00000357339.6:c.771T>A | ENSP00000349896.2:p.Leu257= | |
| ENST00000479522.5:c.*263T>A | ENSP00000424113.1:n.*263T>A | |
| ENST00000484444.5:c.*275T>A | ENSP00000420975.1:n.*275T>A | |
| ENST00000488877.5:c.*275T>A | ENSP00000425159.1:n.*275T>A | |
| ENST00000492756.5:c.662T>A | ENSP00000422453.1:n.662T>A | |
| ENST00000494410.5:c.*192T>A | ENSP00000423755.1:n.*192T>A | |
| ENST00000612663.4:c.*181T>A | ENSP00000477997.2:n.*181T>A | |
| NM_000043.4:c.834T>A , LRG_134t1:c.834T>A | NP_000034.1:p.Leu278= | |
| NM_152871.2:c.771T>A | NP_690610.1:p.Leu257= | |
| NM_152872.2:c.*146T>A | NP_690611.1:n.*146T>A | |
| NR_028033.2:n.1008T>A | ||
| NR_028034.2:n.870T>A | ||
| NR_028035.2:n.933T>A | ||
| NR_028036.2:n.1071T>A | ||
| XM_006717819.2:c.915T>A | XP_006717882.1:p.Leu305= | |
| XM_011539764.1:c.996T>A | XP_011538066.1:p.Leu332= | |
| XM_011539765.1:c.933T>A | XP_011538067.1:p.Leu311= | |
| XM_011539766.1:c.915T>A | XP_011538068.1:p.Leu305= | |
| XM_011539767.1:c.879T>A | XP_011538069.1:p.Leu293= | |
| XR_945732.1:n.902T>A | ||
| XR_945733.1:n.839T>A | ||
| NM_000043.5:c.834T>A | NP_000034.1:p.Leu278= | |
| NM_001320619.1:c.*157T>A | NP_001307548.1:n.*157T>A | |
| NM_152871.3:c.771T>A | NP_690610.1:p.Leu257= | |
| NM_152872.3:c.*146T>A | NP_690611.1:n.*146T>A | |
| NR_028033.3:n.980T>A | ||
| NR_028034.3:n.842T>A | ||
| NR_028035.3:n.905T>A | ||
| NR_028036.3:n.1043T>A | ||
| NR_135313.1:n.960T>A | ||
| NR_135314.1:n.1143T>A | ||
| NR_135315.1:n.896T>A | ||
| XM_006717819.3:c.915T>A | XP_006717882.1:p.Leu305= | |
| XM_011539764.2:c.996T>A | XP_011538066.1:p.Leu332= | |
| XM_011539765.2:c.933T>A | XP_011538067.1:p.Leu311= | |
| XM_011539766.2:c.915T>A | XP_011538068.1:p.Leu305= | |
| XM_011539767.3:c.879T>A | XP_011538069.1:p.Leu293= | |
| XR_945732.3:n.902T>A | ||
| XR_945733.2:n.839T>A | ||
| NM_000043.6:c.834T>A MANE Select | NP_000034.1:p.Leu278= | |
| NM_001320619.2:c.*157T>A | NP_001307548.1:n.*157T>A | |
| NM_152871.4:c.771T>A | NP_690610.1:p.Leu257= | |
| NM_152872.4:c.*146T>A | NP_690611.1:n.*146T>A | |
| NR_028033.4:n.741T>A | ||
| NR_028034.4:n.603T>A | ||
| NR_028035.4:n.666T>A | ||
| NR_028036.4:n.804T>A | ||
| NR_135313.2:n.721T>A | ||
| NR_135314.2:n.1000T>A | ||
| NR_135315.2:n.753T>A |