Canonical Allele Identifier: CA1207934385

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904012G= , CM000663.2:g.173904012G=	GRCh38
NC_000001.10:g.173873150G= , CM000663.1:g.173873150G=	GRCh37
NC_000001.9:g.172139773G=	NCBI36
NG_012462.1:g.18367C= , LRG_577:g.18367C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1272C= MANE Select	ENSP00000356671.3:p.Gly424=
ENST00000367698.3:c.1272C=	ENSP00000356671.3:p.Gly424=
ENST00000617423.4:c.657C=	ENSP00000478688.1:p.Gly219=
NM_000488.3:c.1272C= , LRG_577t1:c.1272C=	NP_000479.1:p.Gly424=
XM_005245198.2:c.1128C=	XP_005245255.1:p.Gly376=
NM_001365052.1:c.1128C=	NP_001351981.1:p.Gly376=
NM_000488.4:c.1272C= MANE Select	NP_000479.1:p.Gly424=
NM_001365052.2:c.1128C=	NP_001351981.1:p.Gly376=
NM_001386302.1:c.1395C=	NP_001373231.1:p.Gly465=
NM_001386303.1:c.1353C=	NP_001373232.1:p.Gly451=
NM_001386304.1:c.1251C=	NP_001373233.1:p.Gly417=
NM_001386305.1:c.1215C=	NP_001373234.1:p.Gly405=
NM_001386306.1:c.1056C=	NP_001373235.1:p.Gly352=