Canonical Allele Identifier: CA211880
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18023
dbSNP Id: rs121909548

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904038C>A , CM000663.2:g.173904038C>A GRCh38
NC_000001.10:g.173873176C>A , CM000663.1:g.173873176C>A GRCh37
NC_000001.9:g.172139799C>A NCBI36
NG_012462.1:g.18341G>T , LRG_577:g.18341G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1246G>T MANE Select ENSP00000356671.3:p.Ala416Ser
ENST00000367698.3:c.1246G>T ENSP00000356671.3:p.Ala416Ser
ENST00000617423.4:c.631G>T ENSP00000478688.1:p.Ala211Ser
NM_000488.3:c.1246G>T , LRG_577t1:c.1246G>T NP_000479.1:p.Ala416Ser
XM_005245198.2:c.1102G>T XP_005245255.1:p.Ala368Ser
NM_001365052.1:c.1102G>T NP_001351981.1:p.Ala368Ser
NM_000488.4:c.1246G>T MANE Select NP_000479.1:p.Ala416Ser
NM_001365052.2:c.1102G>T NP_001351981.1:p.Ala368Ser
NM_001386302.1:c.1369G>T NP_001373231.1:p.Ala457Ser
NM_001386303.1:c.1327G>T NP_001373232.1:p.Ala443Ser
NM_001386304.1:c.1225G>T NP_001373233.1:p.Ala409Ser
NM_001386305.1:c.1189G>T NP_001373234.1:p.Ala397Ser
NM_001386306.1:c.1030G>T NP_001373235.1:p.Ala344Ser