Canonical Allele Identifier: CA1145598774

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910072A= , CM000663.2:g.173910072A=	GRCh38
NC_000001.10:g.173879210A= , CM000663.1:g.173879210A=	GRCh37
NC_000001.9:g.172145833A=	NCBI36
NG_012462.1:g.12307T= , LRG_577:g.12307T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.763-130T= MANE Select	ENSP00000356671.3:n.763-130T=
ENST00000367698.3:c.763-130T=	ENSP00000356671.3:n.763-130T=
ENST00000487183.1:n.414-130T=
ENST00000617423.4:c.559+1792T=	ENSP00000478688.1:n.559+1792T=
NM_000488.3:c.763-130T= , LRG_577t1:c.763-130T=	NP_000479.1:n.763-130T=
XM_005245198.2:c.619-130T=	XP_005245255.1:n.619-130T=
NM_001365052.1:c.619-130T=	NP_001351981.1:n.619-130T=
NM_000488.4:c.763-130T= MANE Select	NP_000479.1:n.763-130T=
NM_001365052.2:c.619-130T=	NP_001351981.1:n.619-130T=
NM_001386302.1:c.886-130T=	NP_001373231.1:n.886-130T=
NM_001386303.1:c.844-130T=	NP_001373232.1:n.844-130T=
NM_001386304.1:c.742-130T=	NP_001373233.1:n.742-130T=
NM_001386305.1:c.763-187T=	NP_001373234.1:n.763-187T=
NM_001386306.1:c.547-130T=	NP_001373235.1:n.547-130T=