Canonical Allele Identifier: CA1207937009

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909829A= , CM000663.2:g.173909829A=	GRCh38
NC_000001.10:g.173878967A= , CM000663.1:g.173878967A=	GRCh37
NC_000001.9:g.172145590A=	NCBI36
NG_012462.1:g.12550T= , LRG_577:g.12550T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.876T= MANE Select	ENSP00000356671.3:p.Tyr292=
ENST00000367698.3:c.876T=	ENSP00000356671.3:p.Tyr292=
ENST00000487183.1:n.527T=
ENST00000617423.4:c.559+2035T=	ENSP00000478688.1:n.559+2035T=
NM_000488.3:c.876T= , LRG_577t1:c.876T=	NP_000479.1:p.Tyr292=
XM_005245198.2:c.732T=	XP_005245255.1:p.Tyr244=
NM_001365052.1:c.732T=	NP_001351981.1:p.Tyr244=
NM_000488.4:c.876T= MANE Select	NP_000479.1:p.Tyr292=
NM_001365052.2:c.732T=	NP_001351981.1:p.Tyr244=
NM_001386302.1:c.999T=	NP_001373231.1:p.Tyr333=
NM_001386303.1:c.957T=	NP_001373232.1:p.Tyr319=
NM_001386304.1:c.855T=	NP_001373233.1:p.Tyr285=
NM_001386305.1:c.819T=	NP_001373234.1:p.Tyr273=
NM_001386306.1:c.660T=	NP_001373235.1:p.Tyr220=