Canonical Allele Identifier: CA407998565
Gene: SIRPG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1630306C>G , CM000682.2:g.1630306C>G GRCh38
NC_000020.10:g.1610952C>G , CM000682.1:g.1610952C>G GRCh37
NC_000020.9:g.1558952C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216927.4:c.749G>C ENSP00000216927.4:p.Gly250Ala
ENST00000303415.7:c.1082G>C MANE Select ENSP00000305529.3:p.Gly361Ala
ENST00000344103.8:c.431G>C ENSP00000342759.4:p.Gly144Ala
ENST00000381580.5:c.983G>C ENSP00000370992.1:p.Gly328Ala
ENST00000381583.6:c.749G>C ENSP00000370995.2:p.Gly250Ala
ENST00000478145.6:n.143G>C
ENST00000497407.2:n.231G>C
NM_001039508.1:c.749G>C NP_001034597.1:p.Gly250Ala
NM_018556.3:c.1082G>C NP_061026.2:p.Gly361Ala
NM_080816.2:c.431G>C NP_543006.2:p.Gly144Ala
XM_005260749.2:c.764G>C XP_005260806.1:p.Gly255Ala
XM_011529286.1:c.983G>C XP_011527588.1:p.Gly328Ala
XM_005260749.4:c.764G>C XP_005260806.1:p.Gly255Ala
XM_011529286.2:c.983G>C XP_011527588.1:p.Gly328Ala
NM_018556.4:c.1082G>C MANE Select NP_061026.2:p.Gly361Ala
NM_080816.3:c.431G>C NP_543006.2:p.Gly144Ala
NM_001039508.2:c.749G>C NP_001034597.1:p.Gly250Ala