Canonical Allele Identifier: CA2651603855
Gene: SIRPG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1630112_1630115dup , CM000682.2:g.1630112_1630115dup GRCh38
NC_000020.10:g.1610758_1610761dup , CM000682.1:g.1610758_1610761dup GRCh37
NC_000020.9:g.1558758_1558761dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303415.7:c.*2+111_*2+114dup MANE Select ENSP00000305529.3:n.*2+111_*2+114dup
ENST00000344103.8:c.*2+111_*2+114dup ENSP00000342759.4:n.*2+111_*2+114dup
ENST00000381580.5:c.*2+111_*2+114dup ENSP00000370992.1:n.*2+111_*2+114dup
ENST00000381583.6:c.*2+111_*2+114dup ENSP00000370995.2:n.*2+111_*2+114dup
ENST00000478145.6:n.227+111_227+114dup
ENST00000497407.2:n.315+111_315+114dup
NM_001039508.1:c.*2+111_*2+114dup NP_001034597.1:n.*2+111_*2+114dup
NM_018556.3:c.*2+111_*2+114dup NP_061026.2:n.*2+111_*2+114dup
NM_080816.2:c.*2+111_*2+114dup NP_543006.2:n.*2+111_*2+114dup
XM_005260749.2:c.*2+111_*2+114dup XP_005260806.1:n.*2+111_*2+114dup
XM_011529286.1:c.*2+111_*2+114dup XP_011527588.1:n.*2+111_*2+114dup
XM_005260749.4:c.*2+111_*2+114dup XP_005260806.1:n.*2+111_*2+114dup
XM_011529286.2:c.*2+111_*2+114dup XP_011527588.1:n.*2+111_*2+114dup
NM_018556.4:c.*2+111_*2+114dup MANE Select NP_061026.2:n.*2+111_*2+114dup
NM_080816.3:c.*2+111_*2+114dup NP_543006.2:n.*2+111_*2+114dup
NM_001039508.2:c.*2+111_*2+114dup NP_001034597.1:n.*2+111_*2+114dup