Canonical Allele Identifier: CA2651603653

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1629570-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1629570A>G , CM000682.2:g.1629570A>G	GRCh38
NC_000020.10:g.1610216A>G , CM000682.1:g.1610216A>G	GRCh37
NC_000020.9:g.1558216A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000303415.7:c.*69T>C MANE Select	ENSP00000305529.3:n.*69T>C
ENST00000344103.8:c.*69T>C	ENSP00000342759.4:n.*69T>C
ENST00000381580.5:c.*69T>C	ENSP00000370992.1:n.*69T>C
ENST00000381583.6:c.*69T>C	ENSP00000370995.2:n.*69T>C
ENST00000478145.6:n.294T>C
ENST00000497407.2:n.382T>C
NM_001039508.1:c.*69T>C	NP_001034597.1:n.*69T>C
NM_018556.3:c.*69T>C	NP_061026.2:n.*69T>C
NM_080816.2:c.*69T>C	NP_543006.2:n.*69T>C
XM_005260749.2:c.*69T>C	XP_005260806.1:n.*69T>C
XM_011529286.1:c.*69T>C	XP_011527588.1:n.*69T>C
XM_005260749.4:c.*69T>C	XP_005260806.1:n.*69T>C
XM_011529286.2:c.*69T>C	XP_011527588.1:n.*69T>C
NM_018556.4:c.*69T>C MANE Select	NP_061026.2:n.*69T>C
NM_080816.3:c.*69T>C	NP_543006.2:n.*69T>C
NM_001039508.2:c.*69T>C	NP_001034597.1:n.*69T>C