Canonical Allele Identifier: CA2577317968
Gene: SIRPG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1630296_1630303dup , CM000682.2:g.1630296_1630303dup GRCh38
NC_000020.10:g.1610942_1610949dup , CM000682.1:g.1610942_1610949dup GRCh37
NC_000020.9:g.1558942_1558949dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216927.4:c.752_759dup ENSP00000216927.4:p.Ser254ArgfsTer11
ENST00000303415.7:c.1085_1092dup MANE Select ENSP00000305529.3:p.Ser365ArgfsTer11
ENST00000344103.8:c.434_441dup ENSP00000342759.4:p.Ser148ArgfsTer11
ENST00000381580.5:c.986_993dup ENSP00000370992.1:p.Ser332ArgfsTer11
ENST00000381583.6:c.752_759dup ENSP00000370995.2:p.Ser254ArgfsTer11
ENST00000478145.6:n.146_153dup
ENST00000497407.2:n.234_241dup
NM_001039508.1:c.752_759dup NP_001034597.1:p.Ser254ArgfsTer11
NM_018556.3:c.1085_1092dup NP_061026.2:p.Ser365ArgfsTer11
NM_080816.2:c.434_441dup NP_543006.2:p.Ser148ArgfsTer11
XM_005260749.2:c.767_774dup XP_005260806.1:p.Ser259ArgfsTer11
XM_011529286.1:c.986_993dup XP_011527588.1:p.Ser332ArgfsTer11
XM_005260749.4:c.767_774dup XP_005260806.1:p.Ser259ArgfsTer11
XM_011529286.2:c.986_993dup XP_011527588.1:p.Ser332ArgfsTer11
NM_018556.4:c.1085_1092dup MANE Select NP_061026.2:p.Ser365ArgfsTer11
NM_080816.3:c.434_441dup NP_543006.2:p.Ser148ArgfsTer11
NM_001039508.2:c.752_759dup NP_001034597.1:p.Ser254ArgfsTer11