Linked Data
ClinVar Variation Id:
178628
dbSNP Id:
rs61731363
ExAC:
10:55782743 A / G
gnomAD v2:
10-55782743-A-G
gnomAD v3:
10-54022983-A-G
gnomAD v4:
10-54022983-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.54022983A>G , CM000672.2:g.54022983A>G | GRCh38 |
| NC_000010.10:g.55782743A>G , CM000672.1:g.55782743A>G | GRCh37 |
| NC_000010.9:g.55452749A>G | NCBI36 |
| NG_009191.2:g.783309T>C | |
| NG_009191.3:g.1611200T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000613657.6:c.2471T>C | ENSP00000482794.1:p.Ile824Thr | |
| ENST00000320301.11:c.2435T>C MANE Plus Clinical | ENSP00000322604.6:p.Ile812Thr | |
| ENST00000395445.6:c.2456T>C | ENSP00000378832.2:p.Ile819Thr | |
| ENST00000613657.5:c.2471T>C | ENSP00000482794.1:p.Ile824Thr | |
| ENST00000642496.1:c.1294T>C | ||
| ENST00000644397.2:c.2435T>C MANE Select | ENSP00000495195.1:p.Ile812Thr | |
| ENST00000320301.10:c.2435T>C | ENSP00000322604.6:p.Ile812Thr | |
| ENST00000361849.7:c.2435T>C | ENSP00000354950.3:p.Ile812Thr | |
| ENST00000373955.5:c.2435T>C | ENSP00000363066.1:p.Ile812Thr | |
| ENST00000373956.7:c.*390T>C | ENSP00000363067.4:n.*390T>C | |
| ENST00000373957.7:c.2450T>C | ENSP00000363068.4:p.Ile817Thr | |
| ENST00000373965.6:c.2435T>C | ENSP00000363076.3:p.Ile812Thr | |
| ENST00000395430.5:c.2435T>C | ENSP00000378818.1:p.Ile812Thr | |
| ENST00000395432.6:c.2324T>C | ENSP00000378820.2:p.Ile775Thr | |
| ENST00000395433.5:c.2369T>C | ENSP00000378821.1:p.Ile790Thr | |
| ENST00000395438.5:c.2435T>C | ENSP00000378826.2:p.Ile812Thr | |
| ENST00000395440.5:c.1305+172700T>C | ENSP00000378827.1:n.1305+172700T>C | |
| ENST00000395442.5:c.1098+190953T>C | ENSP00000378829.1:n.1098+190953T>C | |
| ENST00000395445.5:c.2456T>C | ENSP00000378832.2:p.Ile819Thr | |
| ENST00000395446.5:c.2091+56348T>C | ENSP00000378833.1:n.2091+56348T>C | |
| ENST00000409834.5:c.1268T>C | ENSP00000386693.1:p.Ile423Thr | |
| ENST00000414367.5:c.877-182487T>C | ENSP00000412531.1:n.877-182487T>C | |
| ENST00000414778.5:c.2435T>C | ENSP00000410304.2:p.Ile812Thr | |
| ENST00000437009.5:c.2222T>C | ENSP00000412628.2:p.Ile741Thr | |
| ENST00000448885.5:c.*390T>C | ENSP00000412320.1:n.*390T>C | |
| ENST00000495484.5:c.-24-165720T>C | ENSP00000480780.1:n.-24-165720T>C | |
| ENST00000612394.4:c.2471T>C | ENSP00000482921.1:p.Ile824Thr | |
| ENST00000613657.4:c.2471T>C | ENSP00000482794.1:p.Ile824Thr | |
| ENST00000614895.4:c.2450T>C | ENSP00000478512.1:p.Ile817Thr | |
| ENST00000616114.4:c.2435T>C | ENSP00000483745.1:p.Ile812Thr | |
| ENST00000617051.4:c.2450T>C | ENSP00000484703.1:p.Ile817Thr | |
| ENST00000617271.4:c.2435T>C | ENSP00000478076.1:p.Ile812Thr | |
| ENST00000621708.4:c.2450T>C | ENSP00000484454.1:p.Ile817Thr | |
| ENST00000622048.4:c.2222T>C | ENSP00000482329.1:p.Ile741Thr | |
| NM_001142763.1:c.2450T>C | NP_001136235.1:p.Ile817Thr | |
| NM_001142764.1:c.2435T>C | NP_001136236.1:p.Ile812Thr | |
| NM_001142765.1:c.2222T>C | NP_001136237.1:p.Ile741Thr | |
| NM_001142766.1:c.2435T>C | NP_001136238.1:p.Ile812Thr | |
| NM_001142767.1:c.2324T>C | NP_001136239.1:p.Ile775Thr | |
| NM_001142768.1:c.2369T>C | NP_001136240.1:p.Ile790Thr | |
| NM_001142769.1:c.2471T>C | NP_001136241.1:p.Ile824Thr | |
| NM_001142770.1:c.2435T>C | NP_001136242.1:p.Ile812Thr | |
| NM_001142771.1:c.2450T>C | NP_001136243.1:p.Ile817Thr | |
| NM_001142772.1:c.2435T>C | NP_001136244.1:p.Ile812Thr | |
| NM_001142773.1:c.2369T>C | NP_001136245.1:p.Ile790Thr | |
| NM_033056.3:c.2435T>C | NP_149045.3:p.Ile812Thr | |
| NM_001142769.2:c.2471T>C | NP_001136241.1:p.Ile824Thr | |
| NM_001142770.2:c.2435T>C | NP_001136242.1:p.Ile812Thr | |
| NM_001354404.1:c.2369T>C | NP_001341333.1:p.Ile790Thr | |
| NM_001354411.1:c.2456T>C | NP_001341340.1:p.Ile819Thr | |
| NM_001354420.1:c.2435T>C | NP_001341349.1:p.Ile812Thr | |
| NM_001354429.1:c.2435T>C | NP_001341358.1:p.Ile812Thr | |
| NM_001354430.1:c.2435T>C | NP_001341359.1:p.Ile812Thr | |
| XM_017016573.2:c.2450T>C | XP_016872062.1:p.Ile817Thr | |
| XR_001747192.2:n.3448T>C | ||
| XR_001747193.2:n.3448T>C | ||
| NM_001142763.2:c.2450T>C | NP_001136235.1:p.Ile817Thr | |
| NM_001142764.2:c.2435T>C | NP_001136236.1:p.Ile812Thr | |
| NM_001142765.2:c.2222T>C | NP_001136237.1:p.Ile741Thr | |
| NM_001142766.2:c.2435T>C | NP_001136238.1:p.Ile812Thr | |
| NM_001142768.2:c.2369T>C | NP_001136240.1:p.Ile790Thr | |
| NM_001142769.3:c.2471T>C | NP_001136241.1:p.Ile824Thr | |
| NM_001142770.3:c.2435T>C | NP_001136242.1:p.Ile812Thr | |
| NM_001142771.2:c.2450T>C | NP_001136243.1:p.Ile817Thr | |
| NM_001142772.2:c.2435T>C | NP_001136244.1:p.Ile812Thr | |
| NM_001142773.2:c.2369T>C | NP_001136245.1:p.Ile790Thr | |
| NM_001354411.2:c.2456T>C | NP_001341340.1:p.Ile819Thr | |
| NM_001354420.2:c.2435T>C | NP_001341349.1:p.Ile812Thr | |
| NM_001354429.2:c.2435T>C | NP_001341358.1:p.Ile812Thr | |
| NM_001354430.2:c.2435T>C | NP_001341359.1:p.Ile812Thr | |
| NM_033056.4:c.2435T>C MANE Plus Clinical | NP_149045.3:p.Ile812Thr | |
| NM_001142767.2:c.2324T>C | NP_001136239.1:p.Ile775Thr | |
| NM_001354404.2:c.2369T>C | NP_001341333.1:p.Ile790Thr | |
| NM_001384140.1:c.2435T>C MANE Select | NP_001371069.1:p.Ile812Thr |