Canonical Allele Identifier: CA1251288
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 874664
ClinVar RCV Id: RCV001097815
dbSNP Id: rs376752370

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909639G>A , CM000663.2:g.173909639G>A GRCh38
NC_000001.10:g.173878777G>A , CM000663.1:g.173878777G>A GRCh37
NC_000001.9:g.172145400G>A NCBI36
NG_012462.1:g.12740C>T , LRG_577:g.12740C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1066C>T MANE Select ENSP00000356671.3:p.Arg356Cys
ENST00000367698.3:c.1066C>T ENSP00000356671.3:p.Arg356Cys
ENST00000617423.4:c.560-2146C>T ENSP00000478688.1:n.560-2146C>T
NM_000488.3:c.1066C>T , LRG_577t1:c.1066C>T NP_000479.1:p.Arg356Cys
XM_005245198.2:c.922C>T XP_005245255.1:p.Arg308Cys
NM_001365052.1:c.922C>T NP_001351981.1:p.Arg308Cys
NM_000488.4:c.1066C>T MANE Select NP_000479.1:p.Arg356Cys
NM_001365052.2:c.922C>T NP_001351981.1:p.Arg308Cys
NM_001386302.1:c.1189C>T NP_001373231.1:p.Arg397Cys
NM_001386303.1:c.1147C>T NP_001373232.1:p.Arg383Cys
NM_001386304.1:c.1045C>T NP_001373233.1:p.Arg349Cys
NM_001386305.1:c.1009C>T NP_001373234.1:p.Arg337Cys
NM_001386306.1:c.850C>T NP_001373235.1:p.Arg284Cys