Canonical Allele Identifier: CA1207937010

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909830T= , CM000663.2:g.173909830T=	GRCh38
NC_000001.10:g.173878968T= , CM000663.1:g.173878968T=	GRCh37
NC_000001.9:g.172145591T=	NCBI36
NG_012462.1:g.12549A= , LRG_577:g.12549A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.875A= MANE Select	ENSP00000356671.3:p.Tyr292=
ENST00000367698.3:c.875A=	ENSP00000356671.3:p.Tyr292=
ENST00000487183.1:n.526A=
ENST00000617423.4:c.559+2034A=	ENSP00000478688.1:n.559+2034A=
NM_000488.3:c.875A= , LRG_577t1:c.875A=	NP_000479.1:p.Tyr292=
XM_005245198.2:c.731A=	XP_005245255.1:p.Tyr244=
NM_001365052.1:c.731A=	NP_001351981.1:p.Tyr244=
NM_000488.4:c.875A= MANE Select	NP_000479.1:p.Tyr292=
NM_001365052.2:c.731A=	NP_001351981.1:p.Tyr244=
NM_001386302.1:c.998A=	NP_001373231.1:p.Tyr333=
NM_001386303.1:c.956A=	NP_001373232.1:p.Tyr319=
NM_001386304.1:c.854A=	NP_001373233.1:p.Tyr285=
NM_001386305.1:c.818A=	NP_001373234.1:p.Tyr273=
NM_001386306.1:c.659A=	NP_001373235.1:p.Tyr220=