Canonical Allele Identifier: CA2651604346

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630726-T-TCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630726_1630727insCTG , CM000682.2:g.1630726_1630727insCTG	GRCh38
NC_000020.10:g.1611372_1611373insCTG , CM000682.1:g.1611372_1611373insCTG	GRCh37
NC_000020.9:g.1559372_1559373insCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.749-421_749-420insCAG	ENSP00000216927.4:n.749-421_749-420insCAG
ENST00000303415.7:c.1082-421_1082-420insCAG MANE Select	ENSP00000305529.3:n.1082-421_1082-420insCAG
ENST00000344103.8:c.431-421_431-420insCAG	ENSP00000342759.4:n.431-421_431-420insCAG
ENST00000381580.5:c.983-421_983-420insCAG	ENSP00000370992.1:n.983-421_983-420insCAG
ENST00000381583.6:c.749-421_749-420insCAG	ENSP00000370995.2:n.749-421_749-420insCAG
ENST00000478145.6:n.110_111insCAG
NM_001039508.1:c.749-421_749-420insCAG	NP_001034597.1:n.749-421_749-420insCAG
NM_018556.3:c.1082-421_1082-420insCAG	NP_061026.2:n.1082-421_1082-420insCAG
NM_080816.2:c.431-421_431-420insCAG	NP_543006.2:n.431-421_431-420insCAG
XM_005260749.2:c.764-421_764-420insCAG	XP_005260806.1:n.764-421_764-420insCAG
XM_011529286.1:c.983-421_983-420insCAG	XP_011527588.1:n.983-421_983-420insCAG
XM_005260749.4:c.764-421_764-420insCAG	XP_005260806.1:n.764-421_764-420insCAG
XM_011529286.2:c.983-421_983-420insCAG	XP_011527588.1:n.983-421_983-420insCAG
NM_018556.4:c.1082-421_1082-420insCAG MANE Select	NP_061026.2:n.1082-421_1082-420insCAG
NM_080816.3:c.431-421_431-420insCAG	NP_543006.2:n.431-421_431-420insCAG
NM_001039508.2:c.749-421_749-420insCAG	NP_001034597.1:n.749-421_749-420insCAG