Canonical Allele Identifier: CA2345733478
Gene: SIRPG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1630297G= , CM000682.2:g.1630297G= GRCh38
NC_000020.10:g.1610943G= , CM000682.1:g.1610943G= GRCh37
NC_000020.9:g.1558943G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216927.4:c.758C= ENSP00000216927.4:p.Ser253=
ENST00000303415.7:c.1091C= MANE Select ENSP00000305529.3:p.Ser364=
ENST00000344103.8:c.440C= ENSP00000342759.4:p.Ser147=
ENST00000381580.5:c.992C= ENSP00000370992.1:p.Ser331=
ENST00000381583.6:c.758C= ENSP00000370995.2:p.Ser253=
ENST00000478145.6:n.152C=
ENST00000497407.2:n.240C=
NM_001039508.1:c.758C= NP_001034597.1:p.Ser253=
NM_018556.3:c.1091C= NP_061026.2:p.Ser364=
NM_080816.2:c.440C= NP_543006.2:p.Ser147=
XM_005260749.2:c.773C= XP_005260806.1:p.Ser258=
XM_011529286.1:c.992C= XP_011527588.1:p.Ser331=
XM_005260749.4:c.773C= XP_005260806.1:p.Ser258=
XM_011529286.2:c.992C= XP_011527588.1:p.Ser331=
NM_018556.4:c.1091C= MANE Select NP_061026.2:p.Ser364=
NM_080816.3:c.440C= NP_543006.2:p.Ser147=
NM_001039508.2:c.758C= NP_001034597.1:p.Ser253=