Canonical Allele Identifier: CA2345733465

Gene: SIRPG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630268C= , CM000682.2:g.1630268C=	GRCh38
NC_000020.10:g.1610914C= , CM000682.1:g.1610914C=	GRCh37
NC_000020.9:g.1558914C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.787G=	ENSP00000216927.4:p.Val263=
ENST00000303415.7:c.1120G= MANE Select	ENSP00000305529.3:p.Val374=
ENST00000344103.8:c.469G=	ENSP00000342759.4:p.Val157=
ENST00000381580.5:c.1021G=	ENSP00000370992.1:p.Val341=
ENST00000381583.6:c.787G=	ENSP00000370995.2:p.Val263=
ENST00000478145.6:n.181G=
ENST00000497407.2:n.269G=
NM_001039508.1:c.787G=	NP_001034597.1:p.Val263=
NM_018556.3:c.1120G=	NP_061026.2:p.Val374=
NM_080816.2:c.469G=	NP_543006.2:p.Val157=
XM_005260749.2:c.802G=	XP_005260806.1:p.Val268=
XM_011529286.1:c.1021G=	XP_011527588.1:p.Val341=
XM_005260749.4:c.802G=	XP_005260806.1:p.Val268=
XM_011529286.2:c.1021G=	XP_011527588.1:p.Val341=
NM_018556.4:c.1120G= MANE Select	NP_061026.2:p.Val374=
NM_080816.3:c.469G=	NP_543006.2:p.Val157=
NM_001039508.2:c.787G=	NP_001034597.1:p.Val263=