Canonical Allele Identifier: CA2345733479
Gene: SIRPG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1630298A= , CM000682.2:g.1630298A= GRCh38
NC_000020.10:g.1610944A= , CM000682.1:g.1610944A= GRCh37
NC_000020.9:g.1558944A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216927.4:c.757T= ENSP00000216927.4:p.Ser253=
ENST00000303415.7:c.1090T= MANE Select ENSP00000305529.3:p.Ser364=
ENST00000344103.8:c.439T= ENSP00000342759.4:p.Ser147=
ENST00000381580.5:c.991T= ENSP00000370992.1:p.Ser331=
ENST00000381583.6:c.757T= ENSP00000370995.2:p.Ser253=
ENST00000478145.6:n.151T=
ENST00000497407.2:n.239T=
NM_001039508.1:c.757T= NP_001034597.1:p.Ser253=
NM_018556.3:c.1090T= NP_061026.2:p.Ser364=
NM_080816.2:c.439T= NP_543006.2:p.Ser147=
XM_005260749.2:c.772T= XP_005260806.1:p.Ser258=
XM_011529286.1:c.991T= XP_011527588.1:p.Ser331=
XM_005260749.4:c.772T= XP_005260806.1:p.Ser258=
XM_011529286.2:c.991T= XP_011527588.1:p.Ser331=
NM_018556.4:c.1090T= MANE Select NP_061026.2:p.Ser364=
NM_080816.3:c.439T= NP_543006.2:p.Ser147=
NM_001039508.2:c.757T= NP_001034597.1:p.Ser253=