Linked Data
ClinVar Variation Id:
2575960
ClinVar RCV Id:
RCV003322021
dbSNP Id:
rs775272530
COSMIC:
COSM5945216
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119278248T>A , CM000673.2:g.119278248T>A | GRCh38 |
| NC_000011.9:g.119148958T>A , CM000673.1:g.119148958T>A | GRCh37 |
| NC_000011.8:g.118654168T>A | NCBI36 |
| NG_016808.1:g.76969T>A , LRG_608:g.76969T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700472.1:c.*630T>A | ENSP00000515005.1:n.*630T>A | |
| ENST00000264033.6:c.1178T>A MANE Select | ENSP00000264033.3:p.Ile393Asn | |
| ENST00000637974.1:c.1172T>A | ENSP00000490763.1:p.Ile391Asn | |
| ENST00000264033.5:c.1178T>A | ENSP00000264033.3:p.Ile393Asn | |
| ENST00000634586.1:c.1178T>A | ENSP00000489218.1:p.Ile393Asn | |
| ENST00000634840.1:c.1178T>A | ENSP00000489324.1:p.Ile393Asn | |
| NM_005188.3:c.1178T>A , LRG_608t1:c.1178T>A | NP_005179.2:p.Ile393Asn | |
| XM_011543057.1:c.1178T>A | XP_011541359.1:p.Ile393Asn | |
| NM_005188.4:c.1178T>A MANE Select | NP_005179.2:p.Ile393Asn |