Canonical Allele Identifier: CA210746
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18003
ClinVar RCV Id: RCV000019619
dbSNP Id: rs121909546

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903978C>T , CM000663.2:g.173903978C>T GRCh38
NC_000001.10:g.173873116C>T , CM000663.1:g.173873116C>T GRCh37
NC_000001.9:g.172139739C>T NCBI36
NG_012462.1:g.18401G>A , LRG_577:g.18401G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1306G>A MANE Select ENSP00000356671.3:p.Ala436Thr
ENST00000367698.3:c.1306G>A ENSP00000356671.3:p.Ala436Thr
ENST00000617423.4:c.691G>A ENSP00000478688.1:p.Ala231Thr
NM_000488.3:c.1306G>A , LRG_577t1:c.1306G>A NP_000479.1:p.Ala436Thr
XM_005245198.2:c.1162G>A XP_005245255.1:p.Ala388Thr
NM_001365052.1:c.1162G>A NP_001351981.1:p.Ala388Thr
NM_000488.4:c.1306G>A MANE Select NP_000479.1:p.Ala436Thr
NM_001365052.2:c.1162G>A NP_001351981.1:p.Ala388Thr
NM_001386302.1:c.1429G>A NP_001373231.1:p.Ala477Thr
NM_001386303.1:c.1387G>A NP_001373232.1:p.Ala463Thr
NM_001386304.1:c.1285G>A NP_001373233.1:p.Ala429Thr
NM_001386305.1:c.1249G>A NP_001373234.1:p.Ala417Thr
NM_001386306.1:c.1090G>A NP_001373235.1:p.Ala364Thr