Canonical Allele Identifier: CA2651604004

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630234-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630235del , CM000682.2:g.1630235del	GRCh38
NC_000020.10:g.1610881del , CM000682.1:g.1610881del	GRCh37
NC_000020.9:g.1558881del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.820del	ENSP00000216927.4:p.Gln274ArgfsTer?
ENST00000303415.7:c.1153del MANE Select	ENSP00000305529.3:p.Gln385ArgfsTer?
ENST00000344103.8:c.502del	ENSP00000342759.4:p.Gln168ArgfsTer?
ENST00000381580.5:c.1054del	ENSP00000370992.1:p.Gln352ArgfsTer?
ENST00000381583.6:c.820del	ENSP00000370995.2:p.Gln274ArgfsTer?
ENST00000478145.6:n.214del
ENST00000497407.2:n.302del
NM_001039508.1:c.820del	NP_001034597.1:p.Gln274ArgfsTer?
NM_018556.3:c.1153del	NP_061026.2:p.Gln385ArgfsTer?
NM_080816.2:c.502del	NP_543006.2:p.Gln168ArgfsTer?
XM_005260749.2:c.835del	XP_005260806.1:p.Gln279ArgfsTer?
XM_011529286.1:c.1054del	XP_011527588.1:p.Gln352ArgfsTer?
XM_005260749.4:c.835del	XP_005260806.1:p.Gln279ArgfsTer?
XM_011529286.2:c.1054del	XP_011527588.1:p.Gln352ArgfsTer?
NM_018556.4:c.1153del MANE Select	NP_061026.2:p.Gln385ArgfsTer?
NM_080816.3:c.502del	NP_543006.2:p.Gln168ArgfsTer?
NM_001039508.2:c.820del	NP_001034597.1:p.Gln274ArgfsTer?