Canonical Allele Identifier: CA1207936992
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909783C= , CM000663.2:g.173909783C= GRCh38
NC_000001.10:g.173878921C= , CM000663.1:g.173878921C= GRCh37
NC_000001.9:g.172145544C= NCBI36
NG_012462.1:g.12596G= , LRG_577:g.12596G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.922G= MANE Select ENSP00000356671.3:p.Gly308=
ENST00000367698.3:c.922G= ENSP00000356671.3:p.Gly308=
ENST00000487183.1:n.573G=
ENST00000617423.4:c.559+2081G= ENSP00000478688.1:n.559+2081G=
NM_000488.3:c.922G= , LRG_577t1:c.922G= NP_000479.1:p.Gly308=
XM_005245198.2:c.778G= XP_005245255.1:p.Gly260=
NM_001365052.1:c.778G= NP_001351981.1:p.Gly260=
NM_000488.4:c.922G= MANE Select NP_000479.1:p.Gly308=
NM_001365052.2:c.778G= NP_001351981.1:p.Gly260=
NM_001386302.1:c.1045G= NP_001373231.1:p.Gly349=
NM_001386303.1:c.1003G= NP_001373232.1:p.Gly335=
NM_001386304.1:c.901G= NP_001373233.1:p.Gly301=
NM_001386305.1:c.865G= NP_001373234.1:p.Gly289=
NM_001386306.1:c.706G= NP_001373235.1:p.Gly236=