Canonical Allele Identifier: CA2345733576

Gene: SIRPG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630476A= , CM000682.2:g.1630476A=	GRCh38
NC_000020.10:g.1611122A= , CM000682.1:g.1611122A=	GRCh37
NC_000020.9:g.1559122A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.749-170T=	ENSP00000216927.4:n.749-170T=
ENST00000303415.7:c.1082-170T= MANE Select	ENSP00000305529.3:n.1082-170T=
ENST00000344103.8:c.431-170T=	ENSP00000342759.4:n.431-170T=
ENST00000381580.5:c.983-170T=	ENSP00000370992.1:n.983-170T=
ENST00000381583.6:c.749-170T=	ENSP00000370995.2:n.749-170T=
ENST00000478145.6:n.143-170T=
ENST00000497407.2:n.168T=
NM_001039508.1:c.749-170T=	NP_001034597.1:n.749-170T=
NM_018556.3:c.1082-170T=	NP_061026.2:n.1082-170T=
NM_080816.2:c.431-170T=	NP_543006.2:n.431-170T=
XM_005260749.2:c.764-170T=	XP_005260806.1:n.764-170T=
XM_011529286.1:c.983-170T=	XP_011527588.1:n.983-170T=
XM_005260749.4:c.764-170T=	XP_005260806.1:n.764-170T=
XM_011529286.2:c.983-170T=	XP_011527588.1:n.983-170T=
NM_018556.4:c.1082-170T= MANE Select	NP_061026.2:n.1082-170T=
NM_080816.3:c.431-170T=	NP_543006.2:n.431-170T=
NM_001039508.2:c.749-170T=	NP_001034597.1:n.749-170T=