Canonical Allele Identifier: CA1141581242

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904038C= , CM000663.2:g.173904038C=	GRCh38
NC_000001.10:g.173873176C= , CM000663.1:g.173873176C=	GRCh37
NC_000001.9:g.172139799C=	NCBI36
NG_012462.1:g.18341G= , LRG_577:g.18341G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1246G= MANE Select	ENSP00000356671.3:p.Ala416=
ENST00000367698.3:c.1246G=	ENSP00000356671.3:p.Ala416=
ENST00000617423.4:c.631G=	ENSP00000478688.1:p.Ala211=
NM_000488.3:c.1246G= , LRG_577t1:c.1246G=	NP_000479.1:p.Ala416=
XM_005245198.2:c.1102G=	XP_005245255.1:p.Ala368=
NM_001365052.1:c.1102G=	NP_001351981.1:p.Ala368=
NM_000488.4:c.1246G= MANE Select	NP_000479.1:p.Ala416=
NM_001365052.2:c.1102G=	NP_001351981.1:p.Ala368=
NM_001386302.1:c.1369G=	NP_001373231.1:p.Ala457=
NM_001386303.1:c.1327G=	NP_001373232.1:p.Ala443=
NM_001386304.1:c.1225G=	NP_001373233.1:p.Ala409=
NM_001386305.1:c.1189G=	NP_001373234.1:p.Ala397=
NM_001386306.1:c.1030G=	NP_001373235.1:p.Ala344=