Canonical Allele Identifier: CA1207936364

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173908390T= , CM000663.2:g.173908390T=	GRCh38
NC_000001.10:g.173877528T= , CM000663.1:g.173877528T=	GRCh37
NC_000001.9:g.172144151T=	NCBI36
NG_012462.1:g.13989A= , LRG_577:g.13989A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1154-876A= MANE Select	ENSP00000356671.3:n.1154-876A=
ENST00000367698.3:c.1154-876A=	ENSP00000356671.3:n.1154-876A=
ENST00000617423.4:c.560-897A=	ENSP00000478688.1:n.560-897A=
NM_000488.3:c.1154-876A= , LRG_577t1:c.1154-876A=	NP_000479.1:n.1154-876A=
XM_005245198.2:c.1010-876A=	XP_005245255.1:n.1010-876A=
NM_001365052.1:c.1010-876A=	NP_001351981.1:n.1010-876A=
NM_000488.4:c.1154-876A= MANE Select	NP_000479.1:n.1154-876A=
NM_001365052.2:c.1010-876A=	NP_001351981.1:n.1010-876A=
NM_001386302.1:c.1277-876A=	NP_001373231.1:n.1277-876A=
NM_001386303.1:c.1235-876A=	NP_001373232.1:n.1235-876A=
NM_001386304.1:c.1133-876A=	NP_001373233.1:n.1133-876A=
NM_001386305.1:c.1097-876A=	NP_001373234.1:n.1097-876A=
NM_001386306.1:c.938-876A=	NP_001373235.1:n.938-876A=