Canonical Allele Identifier: CA1207937652

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911386A= , CM000663.2:g.173911386A=	GRCh38
NC_000001.10:g.173880524A= , CM000663.1:g.173880524A=	GRCh37
NC_000001.9:g.172147147A=	NCBI36
NG_012462.1:g.10993T= , LRG_577:g.10993T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.624+413T= MANE Select	ENSP00000356671.3:n.624+413T=
ENST00000367698.3:c.624+413T=	ENSP00000356671.3:n.624+413T=
ENST00000487183.1:n.329+413T=
ENST00000617423.4:c.559+478T=	ENSP00000478688.1:n.559+478T=
NM_000488.3:c.624+413T= , LRG_577t1:c.624+413T=	NP_000479.1:n.624+413T=
XM_005245198.2:c.480+413T=	XP_005245255.1:n.480+413T=
NM_001365052.1:c.480+413T=	NP_001351981.1:n.480+413T=
NM_000488.4:c.624+413T= MANE Select	NP_000479.1:n.624+413T=
NM_001365052.2:c.480+413T=	NP_001351981.1:n.480+413T=
NM_001386302.1:c.624+413T=	NP_001373231.1:n.624+413T=
NM_001386303.1:c.705+413T=	NP_001373232.1:n.705+413T=
NM_001386304.1:c.624+413T=	NP_001373233.1:n.624+413T=
NM_001386305.1:c.624+413T=	NP_001373234.1:n.624+413T=
NM_001386306.1:c.409-495T=	NP_001373235.1:n.409-495T=