Canonical Allele Identifier: CA2345733483
Gene: SIRPG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1630304G= , CM000682.2:g.1630304G= GRCh38
NC_000020.10:g.1610950G= , CM000682.1:g.1610950G= GRCh37
NC_000020.9:g.1558950G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216927.4:c.751C= ENSP00000216927.4:p.Pro251=
ENST00000303415.7:c.1084C= MANE Select ENSP00000305529.3:p.Pro362=
ENST00000344103.8:c.433C= ENSP00000342759.4:p.Pro145=
ENST00000381580.5:c.985C= ENSP00000370992.1:p.Pro329=
ENST00000381583.6:c.751C= ENSP00000370995.2:p.Pro251=
ENST00000478145.6:n.145C=
ENST00000497407.2:n.233C=
NM_001039508.1:c.751C= NP_001034597.1:p.Pro251=
NM_018556.3:c.1084C= NP_061026.2:p.Pro362=
NM_080816.2:c.433C= NP_543006.2:p.Pro145=
XM_005260749.2:c.766C= XP_005260806.1:p.Pro256=
XM_011529286.1:c.985C= XP_011527588.1:p.Pro329=
XM_005260749.4:c.766C= XP_005260806.1:p.Pro256=
XM_011529286.2:c.985C= XP_011527588.1:p.Pro329=
NM_018556.4:c.1084C= MANE Select NP_061026.2:p.Pro362=
NM_080816.3:c.433C= NP_543006.2:p.Pro145=
NM_001039508.2:c.751C= NP_001034597.1:p.Pro251=