Canonical Allele Identifier: CA2651604006
Gene: SIRPG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1630245del , CM000682.2:g.1630245del GRCh38
NC_000020.10:g.1610891del , CM000682.1:g.1610891del GRCh37
NC_000020.9:g.1558891del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216927.4:c.813del ENSP00000216927.4:p.Trp272GlyfsTer?
ENST00000303415.7:c.1146del MANE Select ENSP00000305529.3:p.Trp383GlyfsTer?
ENST00000344103.8:c.495del ENSP00000342759.4:p.Trp166GlyfsTer?
ENST00000381580.5:c.1047del ENSP00000370992.1:p.Trp350GlyfsTer?
ENST00000381583.6:c.813del ENSP00000370995.2:p.Trp272GlyfsTer?
ENST00000478145.6:n.207del
ENST00000497407.2:n.295del
NM_001039508.1:c.813del NP_001034597.1:p.Trp272GlyfsTer?
NM_018556.3:c.1146del NP_061026.2:p.Trp383GlyfsTer?
NM_080816.2:c.495del NP_543006.2:p.Trp166GlyfsTer?
XM_005260749.2:c.828del XP_005260806.1:p.Trp277GlyfsTer?
XM_011529286.1:c.1047del XP_011527588.1:p.Trp350GlyfsTer?
XM_005260749.4:c.828del XP_005260806.1:p.Trp277GlyfsTer?
XM_011529286.2:c.1047del XP_011527588.1:p.Trp350GlyfsTer?
NM_018556.4:c.1146del MANE Select NP_061026.2:p.Trp383GlyfsTer?
NM_080816.3:c.495del NP_543006.2:p.Trp166GlyfsTer?
NM_001039508.2:c.813del NP_001034597.1:p.Trp272GlyfsTer?