Canonical Allele Identifier: CA741594965

Gene: SIRPG

Linked Data

• dbSNP Id: rs1258797921
• MyVariant Identifiers: chr20:g.1611014_1611015insT (hg19) ; chr20:g.1630368_1630369insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630369dup , CM000682.2:g.1630369dup	GRCh38
NC_000020.10:g.1611015dup , CM000682.1:g.1611015dup	GRCh37
NC_000020.9:g.1559015dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.749-63dup	ENSP00000216927.4:n.749-63dup
ENST00000303415.7:c.1082-63dup MANE Select	ENSP00000305529.3:n.1082-63dup
ENST00000344103.8:c.431-63dup	ENSP00000342759.4:n.431-63dup
ENST00000381580.5:c.983-63dup	ENSP00000370992.1:n.983-63dup
ENST00000381583.6:c.749-63dup	ENSP00000370995.2:n.749-63dup
ENST00000478145.6:n.143-63dup
ENST00000497407.2:n.230+45dup
NM_001039508.1:c.749-63dup	NP_001034597.1:n.749-63dup
NM_018556.3:c.1082-63dup	NP_061026.2:n.1082-63dup
NM_080816.2:c.431-63dup	NP_543006.2:n.431-63dup
XM_005260749.2:c.764-63dup	XP_005260806.1:n.764-63dup
XM_011529286.1:c.983-63dup	XP_011527588.1:n.983-63dup
XM_005260749.4:c.764-63dup	XP_005260806.1:n.764-63dup
XM_011529286.2:c.983-63dup	XP_011527588.1:n.983-63dup
NM_018556.4:c.1082-63dup MANE Select	NP_061026.2:n.1082-63dup
NM_080816.3:c.431-63dup	NP_543006.2:n.431-63dup
NM_001039508.2:c.749-63dup	NP_001034597.1:n.749-63dup