Canonical Allele Identifier: CA1207939027
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914865A= , CM000663.2:g.173914865A= GRCh38
NC_000001.10:g.173884003A= , CM000663.1:g.173884003A= GRCh37
NC_000001.9:g.172150626A= NCBI36
NG_012462.1:g.7514T= , LRG_577:g.7514T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.96T= MANE Select ENSP00000356671.3:p.Cys32=
ENST00000367698.3:c.96T= ENSP00000356671.3:p.Cys32=
ENST00000494024.1:n.322T=
ENST00000617423.4:c.96T= ENSP00000478688.1:p.Cys32=
NM_000488.3:c.96T= , LRG_577t1:c.96T= NP_000479.1:p.Cys32=
XM_005245198.2:c.-49T= XP_005245255.1:n.-49T=
NM_001365052.1:c.-49T= NP_001351981.1:n.-49T=
NM_000488.4:c.96T= MANE Select NP_000479.1:p.Cys32=
NM_001365052.2:c.-49T= NP_001351981.1:n.-49T=
NM_001386302.1:c.96T= NP_001373231.1:p.Cys32=
NM_001386303.1:c.177T= NP_001373232.1:p.Cys59=
NM_001386304.1:c.96T= NP_001373233.1:p.Cys32=
NM_001386305.1:c.96T= NP_001373234.1:p.Cys32=
NM_001386306.1:c.96T= NP_001373235.1:p.Cys32=