Canonical Allele Identifier: CA1207937602

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911285A= , CM000663.2:g.173911285A=	GRCh38
NC_000001.10:g.173880423A= , CM000663.1:g.173880423A=	GRCh37
NC_000001.9:g.172147046A=	NCBI36
NG_012462.1:g.11094T= , LRG_577:g.11094T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.625-394T= MANE Select	ENSP00000356671.3:n.625-394T=
ENST00000367698.3:c.625-394T=	ENSP00000356671.3:n.625-394T=
ENST00000487183.1:n.330-448T=
ENST00000617423.4:c.559+579T=	ENSP00000478688.1:n.559+579T=
NM_000488.3:c.625-394T= , LRG_577t1:c.625-394T=	NP_000479.1:n.625-394T=
XM_005245198.2:c.481-394T=	XP_005245255.1:n.481-394T=
NM_001365052.1:c.481-394T=	NP_001351981.1:n.481-394T=
NM_000488.4:c.625-394T= MANE Select	NP_000479.1:n.625-394T=
NM_001365052.2:c.481-394T=	NP_001351981.1:n.481-394T=
NM_001386302.1:c.625-394T=	NP_001373231.1:n.625-394T=
NM_001386303.1:c.706-394T=	NP_001373232.1:n.706-394T=
NM_001386304.1:c.625-394T=	NP_001373233.1:n.625-394T=
NM_001386305.1:c.625-394T=	NP_001373234.1:n.625-394T=
NM_001386306.1:c.409-394T=	NP_001373235.1:n.409-394T=