Canonical Allele Identifier: CA2345733691

Gene: SIRPG

Linked Data

• dbSNP Id: rs2091743114

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630714G>T , CM000682.2:g.1630714G>T	GRCh38
NC_000020.10:g.1611360G>T , CM000682.1:g.1611360G>T	GRCh37
NC_000020.9:g.1559360G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.749-408C>A	ENSP00000216927.4:n.749-408C>A
ENST00000303415.7:c.1082-408C>A MANE Select	ENSP00000305529.3:n.1082-408C>A
ENST00000344103.8:c.431-408C>A	ENSP00000342759.4:n.431-408C>A
ENST00000381580.5:c.983-408C>A	ENSP00000370992.1:n.983-408C>A
ENST00000381583.6:c.749-408C>A	ENSP00000370995.2:n.749-408C>A
ENST00000478145.6:n.123C>A
NM_001039508.1:c.749-408C>A	NP_001034597.1:n.749-408C>A
NM_018556.3:c.1082-408C>A	NP_061026.2:n.1082-408C>A
NM_080816.2:c.431-408C>A	NP_543006.2:n.431-408C>A
XM_005260749.2:c.764-408C>A	XP_005260806.1:n.764-408C>A
XM_011529286.1:c.983-408C>A	XP_011527588.1:n.983-408C>A
XM_005260749.4:c.764-408C>A	XP_005260806.1:n.764-408C>A
XM_011529286.2:c.983-408C>A	XP_011527588.1:n.983-408C>A
NM_018556.4:c.1082-408C>A MANE Select	NP_061026.2:n.1082-408C>A
NM_080816.3:c.431-408C>A	NP_543006.2:n.431-408C>A
NM_001039508.2:c.749-408C>A	NP_001034597.1:n.749-408C>A