Canonical Allele Identifier: CA1141581237

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904013C= , CM000663.2:g.173904013C=	GRCh38
NC_000001.10:g.173873151C= , CM000663.1:g.173873151C=	GRCh37
NC_000001.9:g.172139774C=	NCBI36
NG_012462.1:g.18366G= , LRG_577:g.18366G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1271G= MANE Select	ENSP00000356671.3:p.Gly424=
ENST00000367698.3:c.1271G=	ENSP00000356671.3:p.Gly424=
ENST00000617423.4:c.656G=	ENSP00000478688.1:p.Gly219=
NM_000488.3:c.1271G= , LRG_577t1:c.1271G=	NP_000479.1:p.Gly424=
XM_005245198.2:c.1127G=	XP_005245255.1:p.Gly376=
NM_001365052.1:c.1127G=	NP_001351981.1:p.Gly376=
NM_000488.4:c.1271G= MANE Select	NP_000479.1:p.Gly424=
NM_001365052.2:c.1127G=	NP_001351981.1:p.Gly376=
NM_001386302.1:c.1394G=	NP_001373231.1:p.Gly465=
NM_001386303.1:c.1352G=	NP_001373232.1:p.Gly451=
NM_001386304.1:c.1250G=	NP_001373233.1:p.Gly417=
NM_001386305.1:c.1214G=	NP_001373234.1:p.Gly405=
NM_001386306.1:c.1055G=	NP_001373235.1:p.Gly352=