Canonical Allele Identifier: CA310790912

Gene: SIRPG

Linked Data

• dbSNP Id: rs138191942
• gnomAD v2: 20-1610590-A-G
• gnomAD v3: 20-1629944-A-G
• gnomAD v4: 20-1629944-A-G
• MyVariant Identifiers: chr20:g.1610590A>G (hg19) ; chr20:g.1629944A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1629944A>G , CM000682.2:g.1629944A>G	GRCh38
NC_000020.10:g.1610590A>G , CM000682.1:g.1610590A>G	GRCh37
NC_000020.9:g.1558590A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303415.7:c.*2+278T>C MANE Select	ENSP00000305529.3:n.*2+278T>C
ENST00000344103.8:c.*2+278T>C	ENSP00000342759.4:n.*2+278T>C
ENST00000381580.5:c.*2+278T>C	ENSP00000370992.1:n.*2+278T>C
ENST00000381583.6:c.*2+278T>C	ENSP00000370995.2:n.*2+278T>C
ENST00000478145.6:n.227+278T>C
ENST00000497407.2:n.315+278T>C
NM_001039508.1:c.*2+278T>C	NP_001034597.1:n.*2+278T>C
NM_018556.3:c.*2+278T>C	NP_061026.2:n.*2+278T>C
NM_080816.2:c.*2+278T>C	NP_543006.2:n.*2+278T>C
XM_005260749.2:c.*2+278T>C	XP_005260806.1:n.*2+278T>C
XM_011529286.1:c.*2+278T>C	XP_011527588.1:n.*2+278T>C
XM_005260749.4:c.*2+278T>C	XP_005260806.1:n.*2+278T>C
XM_011529286.2:c.*2+278T>C	XP_011527588.1:n.*2+278T>C
NM_018556.4:c.*2+278T>C MANE Select	NP_061026.2:n.*2+278T>C
NM_080816.3:c.*2+278T>C	NP_543006.2:n.*2+278T>C
NM_001039508.2:c.*2+278T>C	NP_001034597.1:n.*2+278T>C