Canonical Allele Identifier: CA2651603672

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1629585-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1629585_1629586insCC , CM000682.2:g.1629585_1629586insCC	GRCh38
NC_000020.10:g.1610231_1610232insCC , CM000682.1:g.1610231_1610232insCC	GRCh37
NC_000020.9:g.1558231_1558232insCC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000303415.7:c.*53_*54insGG MANE Select	ENSP00000305529.3:n.*53_*54insGG
ENST00000344103.8:c.*53_*54insGG	ENSP00000342759.4:n.*53_*54insGG
ENST00000381580.5:c.*53_*54insGG	ENSP00000370992.1:n.*53_*54insGG
ENST00000381583.6:c.*53_*54insGG	ENSP00000370995.2:n.*53_*54insGG
ENST00000478145.6:n.278_279insGG
ENST00000497407.2:n.366_367insGG
NM_001039508.1:c.*53_*54insGG	NP_001034597.1:n.*53_*54insGG
NM_018556.3:c.*53_*54insGG	NP_061026.2:n.*53_*54insGG
NM_080816.2:c.*53_*54insGG	NP_543006.2:n.*53_*54insGG
XM_005260749.2:c.*53_*54insGG	XP_005260806.1:n.*53_*54insGG
XM_011529286.1:c.*53_*54insGG	XP_011527588.1:n.*53_*54insGG
XM_005260749.4:c.*53_*54insGG	XP_005260806.1:n.*53_*54insGG
XM_011529286.2:c.*53_*54insGG	XP_011527588.1:n.*53_*54insGG
NM_018556.4:c.*53_*54insGG MANE Select	NP_061026.2:n.*53_*54insGG
NM_080816.3:c.*53_*54insGG	NP_543006.2:n.*53_*54insGG
NM_001039508.2:c.*53_*54insGG	NP_001034597.1:n.*53_*54insGG