Canonical Allele Identifier: CA2345733455

Gene: SIRPG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630247C= , CM000682.2:g.1630247C=	GRCh38
NC_000020.10:g.1610893C= , CM000682.1:g.1610893C=	GRCh37
NC_000020.9:g.1558893C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.808G=	ENSP00000216927.4:p.Val270=
ENST00000303415.7:c.1141G= MANE Select	ENSP00000305529.3:p.Val381=
ENST00000344103.8:c.490G=	ENSP00000342759.4:p.Val164=
ENST00000381580.5:c.1042G=	ENSP00000370992.1:p.Val348=
ENST00000381583.6:c.808G=	ENSP00000370995.2:p.Val270=
ENST00000478145.6:n.202G=
ENST00000497407.2:n.290G=
NM_001039508.1:c.808G=	NP_001034597.1:p.Val270=
NM_018556.3:c.1141G=	NP_061026.2:p.Val381=
NM_080816.2:c.490G=	NP_543006.2:p.Val164=
XM_005260749.2:c.823G=	XP_005260806.1:p.Val275=
XM_011529286.1:c.1042G=	XP_011527588.1:p.Val348=
XM_005260749.4:c.823G=	XP_005260806.1:p.Val275=
XM_011529286.2:c.1042G=	XP_011527588.1:p.Val348=
NM_018556.4:c.1141G= MANE Select	NP_061026.2:p.Val381=
NM_080816.3:c.490G=	NP_543006.2:p.Val164=
NM_001039508.2:c.808G=	NP_001034597.1:p.Val270=