Canonical Allele Identifier: CA1207936918

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909626C= , CM000663.2:g.173909626C=	GRCh38
NC_000001.10:g.173878764C= , CM000663.1:g.173878764C=	GRCh37
NC_000001.9:g.172145387C=	NCBI36
NG_012462.1:g.12753G= , LRG_577:g.12753G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1079G= MANE Select	ENSP00000356671.3:p.Gly360=
ENST00000367698.3:c.1079G=	ENSP00000356671.3:p.Gly360=
ENST00000617423.4:c.560-2133G=	ENSP00000478688.1:n.560-2133G=
NM_000488.3:c.1079G= , LRG_577t1:c.1079G=	NP_000479.1:p.Gly360=
XM_005245198.2:c.935G=	XP_005245255.1:p.Gly312=
NM_001365052.1:c.935G=	NP_001351981.1:p.Gly312=
NM_000488.4:c.1079G= MANE Select	NP_000479.1:p.Gly360=
NM_001365052.2:c.935G=	NP_001351981.1:p.Gly312=
NM_001386302.1:c.1202G=	NP_001373231.1:p.Gly401=
NM_001386303.1:c.1160G=	NP_001373232.1:p.Gly387=
NM_001386304.1:c.1058G=	NP_001373233.1:p.Gly353=
NM_001386305.1:c.1022G=	NP_001373234.1:p.Gly341=
NM_001386306.1:c.863G=	NP_001373235.1:p.Gly288=