Canonical Allele Identifier: CA210768
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18020
ClinVar RCV Id: RCV000019636
dbSNP Id: rs121909557

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904044C>T , CM000663.2:g.173904044C>T GRCh38
NC_000001.10:g.173873182C>T , CM000663.1:g.173873182C>T GRCh37
NC_000001.9:g.172139805C>T NCBI36
NG_012462.1:g.18335G>A , LRG_577:g.18335G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1240G>A MANE Select ENSP00000356671.3:p.Ala414Thr
ENST00000367698.3:c.1240G>A ENSP00000356671.3:p.Ala414Thr
ENST00000617423.4:c.625G>A ENSP00000478688.1:p.Ala209Thr
NM_000488.3:c.1240G>A , LRG_577t1:c.1240G>A NP_000479.1:p.Ala414Thr
XM_005245198.2:c.1096G>A XP_005245255.1:p.Ala366Thr
NM_001365052.1:c.1096G>A NP_001351981.1:p.Ala366Thr
NM_000488.4:c.1240G>A MANE Select NP_000479.1:p.Ala414Thr
NM_001365052.2:c.1096G>A NP_001351981.1:p.Ala366Thr
NM_001386302.1:c.1363G>A NP_001373231.1:p.Ala455Thr
NM_001386303.1:c.1321G>A NP_001373232.1:p.Ala441Thr
NM_001386304.1:c.1219G>A NP_001373233.1:p.Ala407Thr
NM_001386305.1:c.1183G>A NP_001373234.1:p.Ala395Thr
NM_001386306.1:c.1024G>A NP_001373235.1:p.Ala342Thr