Canonical Allele Identifier: CA2842410417
Gene: SIRPG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1629914_1629915insA , CM000682.2:g.1629914_1629915insA GRCh38
NC_000020.10:g.1610560_1610561insA , CM000682.1:g.1610560_1610561insA GRCh37
NC_000020.9:g.1558560_1558561insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303415.7:c.*3-279_*3-278insT MANE Select ENSP00000305529.3:n.*3-279_*3-278insT
ENST00000344103.8:c.*3-279_*3-278insT ENSP00000342759.4:n.*3-279_*3-278insT
ENST00000381580.5:c.*3-279_*3-278insT ENSP00000370992.1:n.*3-279_*3-278insT
ENST00000381583.6:c.*3-279_*3-278insT ENSP00000370995.2:n.*3-279_*3-278insT
ENST00000478145.6:n.228-279_228-278insT
ENST00000497407.2:n.316-279_316-278insT
NM_001039508.1:c.*3-279_*3-278insT NP_001034597.1:n.*3-279_*3-278insT
NM_018556.3:c.*3-279_*3-278insT NP_061026.2:n.*3-279_*3-278insT
NM_080816.2:c.*3-279_*3-278insT NP_543006.2:n.*3-279_*3-278insT
XM_005260749.2:c.*3-279_*3-278insT XP_005260806.1:n.*3-279_*3-278insT
XM_011529286.1:c.*3-279_*3-278insT XP_011527588.1:n.*3-279_*3-278insT
XM_005260749.4:c.*3-279_*3-278insT XP_005260806.1:n.*3-279_*3-278insT
XM_011529286.2:c.*3-279_*3-278insT XP_011527588.1:n.*3-279_*3-278insT
NM_018556.4:c.*3-279_*3-278insT MANE Select NP_061026.2:n.*3-279_*3-278insT
NM_080816.3:c.*3-279_*3-278insT NP_543006.2:n.*3-279_*3-278insT
NM_001039508.2:c.*3-279_*3-278insT NP_001034597.1:n.*3-279_*3-278insT