Canonical Allele Identifier: CA1207937021

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909852A= , CM000663.2:g.173909852A=	GRCh38
NC_000001.10:g.173878990A= , CM000663.1:g.173878990A=	GRCh37
NC_000001.9:g.172145613A=	NCBI36
NG_012462.1:g.12527T= , LRG_577:g.12527T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.853T= MANE Select	ENSP00000356671.3:p.Tyr285=
ENST00000367698.3:c.853T=	ENSP00000356671.3:p.Tyr285=
ENST00000487183.1:n.504T=
ENST00000617423.4:c.559+2012T=	ENSP00000478688.1:n.559+2012T=
NM_000488.3:c.853T= , LRG_577t1:c.853T=	NP_000479.1:p.Tyr285=
XM_005245198.2:c.709T=	XP_005245255.1:p.Tyr237=
NM_001365052.1:c.709T=	NP_001351981.1:p.Tyr237=
NM_000488.4:c.853T= MANE Select	NP_000479.1:p.Tyr285=
NM_001365052.2:c.709T=	NP_001351981.1:p.Tyr237=
NM_001386302.1:c.976T=	NP_001373231.1:p.Tyr326=
NM_001386303.1:c.934T=	NP_001373232.1:p.Tyr312=
NM_001386304.1:c.832T=	NP_001373233.1:p.Tyr278=
NM_001386305.1:c.796T=	NP_001373234.1:p.Tyr266=
NM_001386306.1:c.637T=	NP_001373235.1:p.Tyr213=