Canonical Allele Identifier: CA2345733300

Gene: SIRPG

Linked Data

• dbSNP Id: rs2091735479

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1629959G>A , CM000682.2:g.1629959G>A	GRCh38
NC_000020.10:g.1610605G>A , CM000682.1:g.1610605G>A	GRCh37
NC_000020.9:g.1558605G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303415.7:c.*2+263C>T MANE Select	ENSP00000305529.3:n.*2+263C>T
ENST00000344103.8:c.*2+263C>T	ENSP00000342759.4:n.*2+263C>T
ENST00000381580.5:c.*2+263C>T	ENSP00000370992.1:n.*2+263C>T
ENST00000381583.6:c.*2+263C>T	ENSP00000370995.2:n.*2+263C>T
ENST00000478145.6:n.227+263C>T
ENST00000497407.2:n.315+263C>T
NM_001039508.1:c.*2+263C>T	NP_001034597.1:n.*2+263C>T
NM_018556.3:c.*2+263C>T	NP_061026.2:n.*2+263C>T
NM_080816.2:c.*2+263C>T	NP_543006.2:n.*2+263C>T
XM_005260749.2:c.*2+263C>T	XP_005260806.1:n.*2+263C>T
XM_011529286.1:c.*2+263C>T	XP_011527588.1:n.*2+263C>T
XM_005260749.4:c.*2+263C>T	XP_005260806.1:n.*2+263C>T
XM_011529286.2:c.*2+263C>T	XP_011527588.1:n.*2+263C>T
NM_018556.4:c.*2+263C>T MANE Select	NP_061026.2:n.*2+263C>T
NM_080816.3:c.*2+263C>T	NP_543006.2:n.*2+263C>T
NM_001039508.2:c.*2+263C>T	NP_001034597.1:n.*2+263C>T