Canonical Allele Identifier: CA1147668561

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909827C= , CM000663.2:g.173909827C=	GRCh38
NC_000001.10:g.173878965C= , CM000663.1:g.173878965C=	GRCh37
NC_000001.9:g.172145588C=	NCBI36
NG_012462.1:g.12552G= , LRG_577:g.12552G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.878G= MANE Select	ENSP00000356671.3:p.Arg293=
ENST00000367698.3:c.878G=	ENSP00000356671.3:p.Arg293=
ENST00000487183.1:n.529G=
ENST00000617423.4:c.559+2037G=	ENSP00000478688.1:n.559+2037G=
NM_000488.3:c.878G= , LRG_577t1:c.878G=	NP_000479.1:p.Arg293=
XM_005245198.2:c.734G=	XP_005245255.1:p.Arg245=
NM_001365052.1:c.734G=	NP_001351981.1:p.Arg245=
NM_000488.4:c.878G= MANE Select	NP_000479.1:p.Arg293=
NM_001365052.2:c.734G=	NP_001351981.1:p.Arg245=
NM_001386302.1:c.1001G=	NP_001373231.1:p.Arg334=
NM_001386303.1:c.959G=	NP_001373232.1:p.Arg320=
NM_001386304.1:c.857G=	NP_001373233.1:p.Arg286=
NM_001386305.1:c.821G=	NP_001373234.1:p.Arg274=
NM_001386306.1:c.662G=	NP_001373235.1:p.Arg221=