Canonical Allele Identifier: CA1141581221

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910861T= , CM000663.2:g.173910861T=	GRCh38
NC_000001.10:g.173879999T= , CM000663.1:g.173879999T=	GRCh37
NC_000001.9:g.172146622T=	NCBI36
NG_012462.1:g.11518A= , LRG_577:g.11518A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.655A= MANE Select	ENSP00000356671.3:p.Asn219=
ENST00000367698.3:c.655A=	ENSP00000356671.3:p.Asn219=
ENST00000487183.1:n.330-24A=
ENST00000617423.4:c.559+1003A=	ENSP00000478688.1:n.559+1003A=
NM_000488.3:c.655A= , LRG_577t1:c.655A=	NP_000479.1:p.Asn219=
XM_005245198.2:c.511A=	XP_005245255.1:p.Asn171=
NM_001365052.1:c.511A=	NP_001351981.1:p.Asn171=
NM_000488.4:c.655A= MANE Select	NP_000479.1:p.Asn219=
NM_001365052.2:c.511A=	NP_001351981.1:p.Asn171=
NM_001386302.1:c.655A=	NP_001373231.1:p.Asn219=
NM_001386303.1:c.736A=	NP_001373232.1:p.Asn246=
NM_001386304.1:c.655A=	NP_001373233.1:p.Asn219=
NM_001386305.1:c.655A=	NP_001373234.1:p.Asn219=
NM_001386306.1:c.439A=	NP_001373235.1:p.Asn147=