Canonical Allele Identifier: CA2345733458

Gene: SIRPG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630250A= , CM000682.2:g.1630250A=	GRCh38
NC_000020.10:g.1610896A= , CM000682.1:g.1610896A=	GRCh37
NC_000020.9:g.1558896A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.805T=	ENSP00000216927.4:p.Tyr269=
ENST00000303415.7:c.1138T= MANE Select	ENSP00000305529.3:p.Tyr380=
ENST00000344103.8:c.487T=	ENSP00000342759.4:p.Tyr163=
ENST00000381580.5:c.1039T=	ENSP00000370992.1:p.Tyr347=
ENST00000381583.6:c.805T=	ENSP00000370995.2:p.Tyr269=
ENST00000478145.6:n.199T=
ENST00000497407.2:n.287T=
NM_001039508.1:c.805T=	NP_001034597.1:p.Tyr269=
NM_018556.3:c.1138T=	NP_061026.2:p.Tyr380=
NM_080816.2:c.487T=	NP_543006.2:p.Tyr163=
XM_005260749.2:c.820T=	XP_005260806.1:p.Tyr274=
XM_011529286.1:c.1039T=	XP_011527588.1:p.Tyr347=
XM_005260749.4:c.820T=	XP_005260806.1:p.Tyr274=
XM_011529286.2:c.1039T=	XP_011527588.1:p.Tyr347=
NM_018556.4:c.1138T= MANE Select	NP_061026.2:p.Tyr380=
NM_080816.3:c.487T=	NP_543006.2:p.Tyr163=
NM_001039508.2:c.805T=	NP_001034597.1:p.Tyr269=