Linked Data
dbSNP Id:
rs771349174
ExAC:
2:157186332 TGTA / T
gnomAD v2:
2-157186332-TGTA-T
gnomAD v4:
2-156329820-TGTA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.156329824_156329826del , CM000664.2:g.156329824_156329826del | GRCh38 |
| NC_000002.11:g.157186336_157186338del , CM000664.1:g.157186336_157186338del | GRCh37 |
| NC_000002.10:g.156894582_156894584del | NCBI36 |
| NG_011821.1:g.7953_7955del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000421709.2:c.175_177del | ENSP00000388120.2:p.Tyr59del | |
| ENST00000700228.1:c.235_237del | ENSP00000514865.1:p.Tyr79del | |
| ENST00000700231.1:c.364_366del | ENSP00000514868.1:p.Tyr122del | |
| ENST00000339562.9:c.364_366del MANE Select | ENSP00000344479.4:p.Tyr122del | |
| ENST00000675870.1:c.175_177del | ENSP00000502739.1:p.Tyr59del | |
| ENST00000339562.8:c.364_366del | ENSP00000344479.4:p.Tyr122del | |
| ENST00000406048.2:c.208+91_208+93del | ||
| ENST00000409108.6:c.364_366del | ENSP00000386993.2:p.Tyr122del | |
| ENST00000409572.5:c.364_366del | ENSP00000386747.1:p.Tyr122del | |
| ENST00000417764.5:c.175_177del | ENSP00000415632.1:p.Tyr59del | |
| ENST00000417972.5:c.175_177del | ENSP00000394671.1:p.Tyr59del | |
| ENST00000421709.1:c.175_177del | ENSP00000388120.1:p.Tyr59del | |
| ENST00000424077.1:c.364_366del | ENSP00000406808.1:p.Tyr122del | |
| ENST00000426264.5:c.175_177del | ENSP00000389986.1:p.Tyr59del | |
| ENST00000429376.5:c.175_177del | ENSP00000410952.1:p.Tyr59del | |
| NM_006186.3:c.364_366del | NP_006177.1:p.Tyr122del | |
| XM_005246621.2:c.397_399del | XP_005246678.1:p.Tyr133del | |
| XM_005246622.2:c.175_177del | XP_005246679.1:p.Tyr59del | |
| XM_005246623.1:c.175_177del | XP_005246680.1:p.Tyr59del | |
| XM_006712553.2:c.397_399del | XP_006712616.1:p.Tyr133del | |
| XM_011511246.1:c.397_399del | XP_011509548.1:p.Tyr133del | |
| XR_427087.2:n.2570_2572del | ||
| NM_173173.2:c.175_177del | NP_775265.1:p.Tyr59del | |
| XM_005246621.4:c.397_399del | XP_005246678.1:p.Tyr133del | |
| XM_006712553.4:c.397_399del | XP_006712616.1:p.Tyr133del | |
| XM_011511246.2:c.397_399del | XP_011509548.1:p.Tyr133del | |
| XM_017004219.2:c.364_366del | XP_016859708.1:p.Tyr122del | |
| XM_017004220.2:c.364_366del | XP_016859709.1:p.Tyr122del | |
| XR_001738751.2:n.732_734del | ||
| XR_001738752.2:n.554_556del | ||
| XR_427087.4:n.611_613del | ||
| NM_006186.4:c.364_366del MANE Select | NP_006177.1:p.Tyr122del | |
| NM_173173.3:c.175_177del | NP_775265.1:p.Tyr59del |