Canonical Allele Identifier: CA1207937045

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909913C= , CM000663.2:g.173909913C=	GRCh38
NC_000001.10:g.173879051C= , CM000663.1:g.173879051C=	GRCh37
NC_000001.9:g.172145674C=	NCBI36
NG_012462.1:g.12466G= , LRG_577:g.12466G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.792G= MANE Select	ENSP00000356671.3:p.Glu264=
ENST00000367698.3:c.792G=	ENSP00000356671.3:p.Glu264=
ENST00000487183.1:n.443G=
ENST00000617423.4:c.559+1951G=	ENSP00000478688.1:n.559+1951G=
NM_000488.3:c.792G= , LRG_577t1:c.792G=	NP_000479.1:p.Glu264=
XM_005245198.2:c.648G=	XP_005245255.1:p.Glu216=
NM_001365052.1:c.648G=	NP_001351981.1:p.Glu216=
NM_000488.4:c.792G= MANE Select	NP_000479.1:p.Glu264=
NM_001365052.2:c.648G=	NP_001351981.1:p.Glu216=
NM_001386302.1:c.915G=	NP_001373231.1:p.Glu305=
NM_001386303.1:c.873G=	NP_001373232.1:p.Glu291=
NM_001386304.1:c.771G=	NP_001373233.1:p.Glu257=
NM_001386305.1:c.763-28G=	NP_001373234.1:n.763-28G=
NM_001386306.1:c.576G=	NP_001373235.1:p.Glu192=