Canonical Allele Identifier: CA1207936912

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909615T= , CM000663.2:g.173909615T=	GRCh38
NC_000001.10:g.173878753T= , CM000663.1:g.173878753T=	GRCh37
NC_000001.9:g.172145376T=	NCBI36
NG_012462.1:g.12764A= , LRG_577:g.12764A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1090A= MANE Select	ENSP00000356671.3:p.Lys364=
ENST00000367698.3:c.1090A=	ENSP00000356671.3:p.Lys364=
ENST00000617423.4:c.560-2122A=	ENSP00000478688.1:n.560-2122A=
NM_000488.3:c.1090A= , LRG_577t1:c.1090A=	NP_000479.1:p.Lys364=
XM_005245198.2:c.946A=	XP_005245255.1:p.Lys316=
NM_001365052.1:c.946A=	NP_001351981.1:p.Lys316=
NM_000488.4:c.1090A= MANE Select	NP_000479.1:p.Lys364=
NM_001365052.2:c.946A=	NP_001351981.1:p.Lys316=
NM_001386302.1:c.1213A=	NP_001373231.1:p.Lys405=
NM_001386303.1:c.1171A=	NP_001373232.1:p.Lys391=
NM_001386304.1:c.1069A=	NP_001373233.1:p.Lys357=
NM_001386305.1:c.1033A=	NP_001373234.1:p.Lys345=
NM_001386306.1:c.874A=	NP_001373235.1:p.Lys292=