Canonical Allele Identifier: CA1207937007

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909821A= , CM000663.2:g.173909821A=	GRCh38
NC_000001.10:g.173878959A= , CM000663.1:g.173878959A=	GRCh37
NC_000001.9:g.172145582A=	NCBI36
NG_012462.1:g.12558T= , LRG_577:g.12558T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.884T= MANE Select	ENSP00000356671.3:p.Val295=
ENST00000367698.3:c.884T=	ENSP00000356671.3:p.Val295=
ENST00000487183.1:n.535T=
ENST00000617423.4:c.559+2043T=	ENSP00000478688.1:n.559+2043T=
NM_000488.3:c.884T= , LRG_577t1:c.884T=	NP_000479.1:p.Val295=
XM_005245198.2:c.740T=	XP_005245255.1:p.Val247=
NM_001365052.1:c.740T=	NP_001351981.1:p.Val247=
NM_000488.4:c.884T= MANE Select	NP_000479.1:p.Val295=
NM_001365052.2:c.740T=	NP_001351981.1:p.Val247=
NM_001386302.1:c.1007T=	NP_001373231.1:p.Val336=
NM_001386303.1:c.965T=	NP_001373232.1:p.Val322=
NM_001386304.1:c.863T=	NP_001373233.1:p.Val288=
NM_001386305.1:c.827T=	NP_001373234.1:p.Val276=
NM_001386306.1:c.668T=	NP_001373235.1:p.Val223=