Canonical Allele Identifier: CA2815016869
Gene: SIRPG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1630546dup , CM000682.2:g.1630546dup GRCh38
NC_000020.10:g.1611192dup , CM000682.1:g.1611192dup GRCh37
NC_000020.9:g.1559192dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216927.4:c.749-236dup ENSP00000216927.4:n.749-236dup
ENST00000303415.7:c.1082-236dup MANE Select ENSP00000305529.3:n.1082-236dup
ENST00000344103.8:c.431-236dup ENSP00000342759.4:n.431-236dup
ENST00000381580.5:c.983-236dup ENSP00000370992.1:n.983-236dup
ENST00000381583.6:c.749-236dup ENSP00000370995.2:n.749-236dup
ENST00000478145.6:n.142+153dup
ENST00000497407.2:n.102dup
NM_001039508.1:c.749-236dup NP_001034597.1:n.749-236dup
NM_018556.3:c.1082-236dup NP_061026.2:n.1082-236dup
NM_080816.2:c.431-236dup NP_543006.2:n.431-236dup
XM_005260749.2:c.764-236dup XP_005260806.1:n.764-236dup
XM_011529286.1:c.983-236dup XP_011527588.1:n.983-236dup
XM_005260749.4:c.764-236dup XP_005260806.1:n.764-236dup
XM_011529286.2:c.983-236dup XP_011527588.1:n.983-236dup
NM_018556.4:c.1082-236dup MANE Select NP_061026.2:n.1082-236dup
NM_080816.3:c.431-236dup NP_543006.2:n.431-236dup
NM_001039508.2:c.749-236dup NP_001034597.1:n.749-236dup