Linked Data
ClinVar Variation Id:
18443
dbSNP Id:
rs786205084
gnomAD v2:
2-71895972-G-A
gnomAD v4:
2-71668842-G-A
PubMed:
PMID:20535123
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71668842G>A , CM000664.2:g.71668842G>A | GRCh38 |
| NC_000002.11:g.71895972G>A , CM000664.1:g.71895972G>A | GRCh37 |
| NC_000002.10:g.71749480G>A | NCBI36 |
| NG_008694.1:g.220220G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.2960G>A | ENSP00000513536.1:p.Arg987Lys | |
| ENST00000698058.1:c.2177G>A | ENSP00000513537.1:p.Arg726Lys | |
| ENST00000698059.1:c.2285G>A | ENSP00000513538.1:p.Arg762Lys | |
| ENST00000258104.8:c.5429G>A MANE Plus Clinical | ENSP00000258104.3:p.Arg1810Lys | |
| ENST00000410020.8:c.5546G>A MANE Select | ENSP00000386881.3:p.Arg1849Lys | |
| ENST00000258104.7:c.5429G>A | ENSP00000258104.3:p.Arg1810Lys | |
| ENST00000394120.6:c.5432G>A | ENSP00000377678.2:p.Arg1811Lys | |
| ENST00000409366.5:c.5495G>A | ENSP00000386512.1:p.Arg1832Lys | |
| ENST00000409582.7:c.5543G>A | ENSP00000386547.3:p.Arg1848Lys | |
| ENST00000409651.5:c.5525G>A | ENSP00000386683.1:p.Arg1842Lys | |
| ENST00000409744.5:c.5453G>A | ENSP00000386285.1:p.Arg1818Lys | |
| ENST00000409762.5:c.5480G>A | ENSP00000387137.1:p.Arg1827Lys | |
| ENST00000410020.7:c.5546G>A | ENSP00000386881.3:p.Arg1849Lys | |
| ENST00000410041.1:c.5483G>A | ENSP00000386617.1:p.Arg1828Lys | |
| ENST00000413539.6:c.5522G>A | ENSP00000407046.2:p.Arg1841Lys | |
| ENST00000429174.6:c.5492G>A | ENSP00000398305.2:p.Arg1831Lys | |
| ENST00000479049.6:n.2314G>A | ||
| NM_001130455.1:c.5432G>A | NP_001123927.1:p.Arg1811Lys | |
| NM_001130976.1:c.5387G>A | NP_001124448.1:p.Arg1796Lys | |
| NM_001130977.1:c.5450G>A | NP_001124449.1:p.Arg1817Lys | |
| NM_001130978.1:c.5492G>A | NP_001124450.1:p.Arg1831Lys | |
| NM_001130979.1:c.5522G>A | NP_001124451.1:p.Arg1841Lys | |
| NM_001130980.1:c.5480G>A | NP_001124452.1:p.Arg1827Lys | |
| NM_001130981.1:c.5543G>A | NP_001124453.1:p.Arg1848Lys | |
| NM_001130982.1:c.5525G>A | NP_001124454.1:p.Arg1842Lys | |
| NM_001130983.1:c.5495G>A | NP_001124455.1:p.Arg1832Lys | |
| NM_001130984.1:c.5453G>A | NP_001124456.1:p.Arg1818Lys | |
| NM_001130985.1:c.5483G>A | NP_001124457.1:p.Arg1828Lys | |
| NM_001130986.1:c.5390G>A | NP_001124458.1:p.Arg1797Lys | |
| NM_001130987.1:c.5546G>A | NP_001124459.1:p.Arg1849Lys | |
| NM_003494.3:c.5429G>A | NP_003485.1:p.Arg1810Lys | |
| XM_005264584.3:c.5588G>A | XP_005264641.1:p.Arg1863Lys | |
| XM_005264585.3:c.5585G>A | XP_005264642.1:p.Arg1862Lys | |
| XM_005264584.4:c.5588G>A | XP_005264641.1:p.Arg1863Lys | |
| XM_005264585.5:c.5585G>A | XP_005264642.1:p.Arg1862Lys | |
| NM_001130987.2:c.5546G>A MANE Select | NP_001124459.1:p.Arg1849Lys | |
| NM_001130455.2:c.5432G>A | NP_001123927.1:p.Arg1811Lys | |
| NM_001130976.2:c.5387G>A | NP_001124448.1:p.Arg1796Lys | |
| NM_001130977.2:c.5450G>A | NP_001124449.1:p.Arg1817Lys | |
| NM_001130978.2:c.5492G>A | NP_001124450.1:p.Arg1831Lys | |
| NM_001130979.2:c.5522G>A | NP_001124451.1:p.Arg1841Lys | |
| NM_001130980.2:c.5480G>A | NP_001124452.1:p.Arg1827Lys | |
| NM_001130981.2:c.5543G>A | NP_001124453.1:p.Arg1848Lys | |
| NM_001130982.2:c.5525G>A | NP_001124454.1:p.Arg1842Lys | |
| NM_001130983.2:c.5495G>A | NP_001124455.1:p.Arg1832Lys | |
| NM_001130984.2:c.5453G>A | NP_001124456.1:p.Arg1818Lys | |
| NM_001130985.2:c.5483G>A | NP_001124457.1:p.Arg1828Lys | |
| NM_001130986.2:c.5390G>A | NP_001124458.1:p.Arg1797Lys | |
| NM_003494.4:c.5429G>A MANE Plus Clinical | NP_003485.1:p.Arg1810Lys |