Canonical Allele Identifier: CA1207936926

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909644C= , CM000663.2:g.173909644C=	GRCh38
NC_000001.10:g.173878782C= , CM000663.1:g.173878782C=	GRCh37
NC_000001.9:g.172145405C=	NCBI36
NG_012462.1:g.12735G= , LRG_577:g.12735G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1061G= MANE Select	ENSP00000356671.3:p.Arg354=
ENST00000367698.3:c.1061G=	ENSP00000356671.3:p.Arg354=
ENST00000617423.4:c.560-2151G=	ENSP00000478688.1:n.560-2151G=
NM_000488.3:c.1061G= , LRG_577t1:c.1061G=	NP_000479.1:p.Arg354=
XM_005245198.2:c.917G=	XP_005245255.1:p.Arg306=
NM_001365052.1:c.917G=	NP_001351981.1:p.Arg306=
NM_000488.4:c.1061G= MANE Select	NP_000479.1:p.Arg354=
NM_001365052.2:c.917G=	NP_001351981.1:p.Arg306=
NM_001386302.1:c.1184G=	NP_001373231.1:p.Arg395=
NM_001386303.1:c.1142G=	NP_001373232.1:p.Arg381=
NM_001386304.1:c.1040G=	NP_001373233.1:p.Arg347=
NM_001386305.1:c.1004G=	NP_001373234.1:p.Arg335=
NM_001386306.1:c.845G=	NP_001373235.1:p.Arg282=