Canonical Allele Identifier: CA1207938990
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914793G= , CM000663.2:g.173914793G= GRCh38
NC_000001.10:g.173883931G= , CM000663.1:g.173883931G= GRCh37
NC_000001.9:g.172150554G= NCBI36
NG_012462.1:g.7586C= , LRG_577:g.7586C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.168C= MANE Select ENSP00000356671.3:p.Arg56=
ENST00000367698.3:c.168C= ENSP00000356671.3:p.Arg56=
ENST00000494024.1:n.394C=
ENST00000617423.4:c.168C= ENSP00000478688.1:p.Arg56=
NM_000488.3:c.168C= , LRG_577t1:c.168C= NP_000479.1:p.Arg56=
XM_005245198.2:c.24C= XP_005245255.1:p.Arg8=
NM_001365052.1:c.24C= NP_001351981.1:p.Arg8=
NM_000488.4:c.168C= MANE Select NP_000479.1:p.Arg56=
NM_001365052.2:c.24C= NP_001351981.1:p.Arg8=
NM_001386302.1:c.168C= NP_001373231.1:p.Arg56=
NM_001386303.1:c.249C= NP_001373232.1:p.Arg83=
NM_001386304.1:c.168C= NP_001373233.1:p.Arg56=
NM_001386305.1:c.168C= NP_001373234.1:p.Arg56=
NM_001386306.1:c.168C= NP_001373235.1:p.Arg56=