Linked Data
ClinVar Variation Id:
251812
ClinVar RCV Id:
RCV000237982
dbSNP Id:
rs879254879
ERepo:
CA10585425/MONDO:0007750/013
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11113537C>A , CM000681.2:g.11113537C>A | GRCh38 |
| NC_000019.9:g.11224213C>A , CM000681.1:g.11224213C>A | GRCh37 |
| NC_000019.8:g.11085213C>A | NCBI36 |
| NG_009060.1:g.29157C>A , LRG_274:g.29157C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.1619C>A | ENSP00000252444.6:p.Thr540Asn | |
| ENST00000559340.2:c.1361C>A | ENSP00000453696.2:p.Thr454Asn | |
| ENST00000560467.2:c.1241C>A | ENSP00000453513.2:p.Thr414Asn | |
| ENST00000558518.6:c.1361C>A MANE Select | ENSP00000454071.1:p.Thr454Asn | |
| ENST00000252444.9:c.1615C>A | ||
| ENST00000455727.6:c.857C>A | ENSP00000397829.2:p.Thr286Asn | |
| ENST00000535915.5:c.1238C>A | ENSP00000440520.1:p.Thr413Asn | |
| ENST00000545707.5:c.980C>A | ENSP00000437639.1:p.Thr327Asn | |
| ENST00000557933.5:c.1361C>A | ENSP00000453557.1:p.Thr454Asn | |
| ENST00000558013.5:c.1361C>A | ENSP00000453346.1:p.Thr454Asn | |
| ENST00000558518.5:c.1361C>A | ENSP00000454071.1:p.Thr454Asn | |
| ENST00000559340.1:c.82C>A | ||
| ENST00000560467.1:c.841C>A | ||
| NM_000527.4:c.1361C>A , LRG_274t1:c.1361C>A | NP_000518.1:p.Thr454Asn | |
| NM_001195798.1:c.1361C>A | NP_001182727.1:p.Thr454Asn | |
| NM_001195799.1:c.1238C>A | NP_001182728.1:p.Thr413Asn | |
| NM_001195800.1:c.857C>A | NP_001182729.1:p.Thr286Asn | |
| NM_001195803.1:c.980C>A | NP_001182732.1:p.Thr327Asn | |
| XM_011528010.1:c.1361C>A | XP_011526312.1:p.Thr454Asn | |
| XM_011528011.1:c.980C>A | XP_011526313.1:p.Thr327Asn | |
| XR_244074.2:n.1511C>A | ||
| XM_011528010.2:c.1361C>A | XP_011526312.1:p.Thr454Asn | |
| XR_001753685.2:n.1478C>A | ||
| XR_001753686.2:n.1478C>A | ||
| NM_000527.5:c.1361C>A MANE Select | NP_000518.1:p.Thr454Asn | |
| NM_001195798.2:c.1361C>A | NP_001182727.1:p.Thr454Asn | |
| NM_001195799.2:c.1238C>A | NP_001182728.1:p.Thr413Asn | |
| NM_001195800.2:c.857C>A | NP_001182729.1:p.Thr286Asn | |
| NM_001195803.2:c.980C>A | NP_001182732.1:p.Thr327Asn |