Canonical Allele Identifier: CA1207936997

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909798C= , CM000663.2:g.173909798C=	GRCh38
NC_000001.10:g.173878936C= , CM000663.1:g.173878936C=	GRCh37
NC_000001.9:g.172145559C=	NCBI36
NG_012462.1:g.12581G= , LRG_577:g.12581G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.907G= MANE Select	ENSP00000356671.3:p.Glu303=
ENST00000367698.3:c.907G=	ENSP00000356671.3:p.Glu303=
ENST00000487183.1:n.558G=
ENST00000617423.4:c.559+2066G=	ENSP00000478688.1:n.559+2066G=
NM_000488.3:c.907G= , LRG_577t1:c.907G=	NP_000479.1:p.Glu303=
XM_005245198.2:c.763G=	XP_005245255.1:p.Glu255=
NM_001365052.1:c.763G=	NP_001351981.1:p.Glu255=
NM_000488.4:c.907G= MANE Select	NP_000479.1:p.Glu303=
NM_001365052.2:c.763G=	NP_001351981.1:p.Glu255=
NM_001386302.1:c.1030G=	NP_001373231.1:p.Glu344=
NM_001386303.1:c.988G=	NP_001373232.1:p.Glu330=
NM_001386304.1:c.886G=	NP_001373233.1:p.Glu296=
NM_001386305.1:c.850G=	NP_001373234.1:p.Glu284=
NM_001386306.1:c.691G=	NP_001373235.1:p.Glu231=