Canonical Allele Identifier: CA2345733301
Gene: SIRPG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1629960_1629961delinsAC , CM000682.2:g.1629960_1629961delinsAC GRCh38
NC_000020.10:g.1610606_1610607delinsAC , CM000682.1:g.1610606_1610607delinsAC GRCh37
NC_000020.9:g.1558606_1558607delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303415.7:c.*2+261_*2+262delinsGT MANE Select ENSP00000305529.3:n.*2+261_*2+262delinsGT
ENST00000344103.8:c.*2+261_*2+262delinsGT ENSP00000342759.4:n.*2+261_*2+262delinsGT
ENST00000381580.5:c.*2+261_*2+262delinsGT ENSP00000370992.1:n.*2+261_*2+262delinsGT
ENST00000381583.6:c.*2+261_*2+262delinsGT ENSP00000370995.2:n.*2+261_*2+262delinsGT
ENST00000478145.6:n.227+261_227+262delinsGT
ENST00000497407.2:n.315+261_315+262delinsGT
NM_001039508.1:c.*2+261_*2+262delinsGT NP_001034597.1:n.*2+261_*2+262delinsGT
NM_018556.3:c.*2+261_*2+262delinsGT NP_061026.2:n.*2+261_*2+262delinsGT
NM_080816.2:c.*2+261_*2+262delinsGT NP_543006.2:n.*2+261_*2+262delinsGT
XM_005260749.2:c.*2+261_*2+262delinsGT XP_005260806.1:n.*2+261_*2+262delinsGT
XM_011529286.1:c.*2+261_*2+262delinsGT XP_011527588.1:n.*2+261_*2+262delinsGT
XM_005260749.4:c.*2+261_*2+262delinsGT XP_005260806.1:n.*2+261_*2+262delinsGT
XM_011529286.2:c.*2+261_*2+262delinsGT XP_011527588.1:n.*2+261_*2+262delinsGT
NM_018556.4:c.*2+261_*2+262delinsGT MANE Select NP_061026.2:n.*2+261_*2+262delinsGT
NM_080816.3:c.*2+261_*2+262delinsGT NP_543006.2:n.*2+261_*2+262delinsGT
NM_001039508.2:c.*2+261_*2+262delinsGT NP_001034597.1:n.*2+261_*2+262delinsGT