Canonical Allele Identifier: CA2345733247
Gene: SIRPG HGNC NCBI

Linked Data

dbSNP Id: rs2091734581

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1629853_1629869del , CM000682.2:g.1629853_1629869del GRCh38
NC_000020.10:g.1610499_1610515del , CM000682.1:g.1610499_1610515del GRCh37
NC_000020.9:g.1558499_1558515del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303415.7:c.*3-231_*3-215del MANE Select ENSP00000305529.3:n.*3-231_*3-215del
ENST00000344103.8:c.*3-231_*3-215del ENSP00000342759.4:n.*3-231_*3-215del
ENST00000381580.5:c.*3-231_*3-215del ENSP00000370992.1:n.*3-231_*3-215del
ENST00000381583.6:c.*3-231_*3-215del ENSP00000370995.2:n.*3-231_*3-215del
ENST00000478145.6:n.228-231_228-215del
ENST00000497407.2:n.316-231_316-215del
NM_001039508.1:c.*3-231_*3-215del NP_001034597.1:n.*3-231_*3-215del
NM_018556.3:c.*3-231_*3-215del NP_061026.2:n.*3-231_*3-215del
NM_080816.2:c.*3-231_*3-215del NP_543006.2:n.*3-231_*3-215del
XM_005260749.2:c.*3-231_*3-215del XP_005260806.1:n.*3-231_*3-215del
XM_011529286.1:c.*3-231_*3-215del XP_011527588.1:n.*3-231_*3-215del
XM_005260749.4:c.*3-231_*3-215del XP_005260806.1:n.*3-231_*3-215del
XM_011529286.2:c.*3-231_*3-215del XP_011527588.1:n.*3-231_*3-215del
NM_018556.4:c.*3-231_*3-215del MANE Select NP_061026.2:n.*3-231_*3-215del
NM_080816.3:c.*3-231_*3-215del NP_543006.2:n.*3-231_*3-215del
NM_001039508.2:c.*3-231_*3-215del NP_001034597.1:n.*3-231_*3-215del