Canonical Allele Identifier: CA2651604051
Gene: SIRPG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1630357_1630366del , CM000682.2:g.1630357_1630366del GRCh38
NC_000020.10:g.1611003_1611012del , CM000682.1:g.1611003_1611012del GRCh37
NC_000020.9:g.1559003_1559012del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216927.4:c.749-60_749-51del ENSP00000216927.4:n.749-60_749-51del
ENST00000303415.7:c.1082-60_1082-51del MANE Select ENSP00000305529.3:n.1082-60_1082-51del
ENST00000344103.8:c.431-60_431-51del ENSP00000342759.4:n.431-60_431-51del
ENST00000381580.5:c.983-60_983-51del ENSP00000370992.1:n.983-60_983-51del
ENST00000381583.6:c.749-60_749-51del ENSP00000370995.2:n.749-60_749-51del
ENST00000478145.6:n.143-60_143-51del
ENST00000497407.2:n.230+48_231-51del
NM_001039508.1:c.749-60_749-51del NP_001034597.1:n.749-60_749-51del
NM_018556.3:c.1082-60_1082-51del NP_061026.2:n.1082-60_1082-51del
NM_080816.2:c.431-60_431-51del NP_543006.2:n.431-60_431-51del
XM_005260749.2:c.764-60_764-51del XP_005260806.1:n.764-60_764-51del
XM_011529286.1:c.983-60_983-51del XP_011527588.1:n.983-60_983-51del
XM_005260749.4:c.764-60_764-51del XP_005260806.1:n.764-60_764-51del
XM_011529286.2:c.983-60_983-51del XP_011527588.1:n.983-60_983-51del
NM_018556.4:c.1082-60_1082-51del MANE Select NP_061026.2:n.1082-60_1082-51del
NM_080816.3:c.431-60_431-51del NP_543006.2:n.431-60_431-51del
NM_001039508.2:c.749-60_749-51del NP_001034597.1:n.749-60_749-51del