Canonical Allele Identifier: CA2589564273

Gene: SIRPG

Linked Data

• gnomAD v3: 20-1630707-A-C
• gnomAD v4: 20-1630707-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630707A>C , CM000682.2:g.1630707A>C	GRCh38
NC_000020.10:g.1611353A>C , CM000682.1:g.1611353A>C	GRCh37
NC_000020.9:g.1559353A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.749-401T>G	ENSP00000216927.4:n.749-401T>G
ENST00000303415.7:c.1082-401T>G MANE Select	ENSP00000305529.3:n.1082-401T>G
ENST00000344103.8:c.431-401T>G	ENSP00000342759.4:n.431-401T>G
ENST00000381580.5:c.983-401T>G	ENSP00000370992.1:n.983-401T>G
ENST00000381583.6:c.749-401T>G	ENSP00000370995.2:n.749-401T>G
ENST00000478145.6:n.130T>G
NM_001039508.1:c.749-401T>G	NP_001034597.1:n.749-401T>G
NM_018556.3:c.1082-401T>G	NP_061026.2:n.1082-401T>G
NM_080816.2:c.431-401T>G	NP_543006.2:n.431-401T>G
XM_005260749.2:c.764-401T>G	XP_005260806.1:n.764-401T>G
XM_011529286.1:c.983-401T>G	XP_011527588.1:n.983-401T>G
XM_005260749.4:c.764-401T>G	XP_005260806.1:n.764-401T>G
XM_011529286.2:c.983-401T>G	XP_011527588.1:n.983-401T>G
NM_018556.4:c.1082-401T>G MANE Select	NP_061026.2:n.1082-401T>G
NM_080816.3:c.431-401T>G	NP_543006.2:n.431-401T>G
NM_001039508.2:c.749-401T>G	NP_001034597.1:n.749-401T>G