Canonical Allele Identifier: CA2345733240
Gene: SIRPG HGNC NCBI

Linked Data

dbSNP Id: rs2091734509

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1629835_1629836dup , CM000682.2:g.1629835_1629836dup GRCh38
NC_000020.10:g.1610481_1610482dup , CM000682.1:g.1610481_1610482dup GRCh37
NC_000020.9:g.1558481_1558482dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303415.7:c.*3-198_*3-197dup MANE Select ENSP00000305529.3:n.*3-198_*3-197dup
ENST00000344103.8:c.*3-198_*3-197dup ENSP00000342759.4:n.*3-198_*3-197dup
ENST00000381580.5:c.*3-198_*3-197dup ENSP00000370992.1:n.*3-198_*3-197dup
ENST00000381583.6:c.*3-198_*3-197dup ENSP00000370995.2:n.*3-198_*3-197dup
ENST00000478145.6:n.228-198_228-197dup
ENST00000497407.2:n.316-198_316-197dup
NM_001039508.1:c.*3-198_*3-197dup NP_001034597.1:n.*3-198_*3-197dup
NM_018556.3:c.*3-198_*3-197dup NP_061026.2:n.*3-198_*3-197dup
NM_080816.2:c.*3-198_*3-197dup NP_543006.2:n.*3-198_*3-197dup
XM_005260749.2:c.*3-198_*3-197dup XP_005260806.1:n.*3-198_*3-197dup
XM_011529286.1:c.*3-198_*3-197dup XP_011527588.1:n.*3-198_*3-197dup
XM_005260749.4:c.*3-198_*3-197dup XP_005260806.1:n.*3-198_*3-197dup
XM_011529286.2:c.*3-198_*3-197dup XP_011527588.1:n.*3-198_*3-197dup
NM_018556.4:c.*3-198_*3-197dup MANE Select NP_061026.2:n.*3-198_*3-197dup
NM_080816.3:c.*3-198_*3-197dup NP_543006.2:n.*3-198_*3-197dup
NM_001039508.2:c.*3-198_*3-197dup NP_001034597.1:n.*3-198_*3-197dup