Canonical Allele Identifier: CA1141581240

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904028G= , CM000663.2:g.173904028G=	GRCh38
NC_000001.10:g.173873166G= , CM000663.1:g.173873166G=	GRCh37
NC_000001.9:g.172139789G=	NCBI36
NG_012462.1:g.18351C= , LRG_577:g.18351C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1256C= MANE Select	ENSP00000356671.3:p.Ala419=
ENST00000367698.3:c.1256C=	ENSP00000356671.3:p.Ala419=
ENST00000617423.4:c.641C=	ENSP00000478688.1:p.Ala214=
NM_000488.3:c.1256C= , LRG_577t1:c.1256C=	NP_000479.1:p.Ala419=
XM_005245198.2:c.1112C=	XP_005245255.1:p.Ala371=
NM_001365052.1:c.1112C=	NP_001351981.1:p.Ala371=
NM_000488.4:c.1256C= MANE Select	NP_000479.1:p.Ala419=
NM_001365052.2:c.1112C=	NP_001351981.1:p.Ala371=
NM_001386302.1:c.1379C=	NP_001373231.1:p.Ala460=
NM_001386303.1:c.1337C=	NP_001373232.1:p.Ala446=
NM_001386304.1:c.1235C=	NP_001373233.1:p.Ala412=
NM_001386305.1:c.1199C=	NP_001373234.1:p.Ala400=
NM_001386306.1:c.1040C=	NP_001373235.1:p.Ala347=