Canonical Allele Identifier: CA2651604009

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630302-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630305del , CM000682.2:g.1630305del	GRCh38
NC_000020.10:g.1610951del , CM000682.1:g.1610951del	GRCh37
NC_000020.9:g.1558951del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.752del	ENSP00000216927.4:p.Pro251ArgfsTer11
ENST00000303415.7:c.1085del MANE Select	ENSP00000305529.3:p.Pro362ArgfsTer11
ENST00000344103.8:c.434del	ENSP00000342759.4:p.Pro145ArgfsTer11
ENST00000381580.5:c.986del	ENSP00000370992.1:p.Pro329ArgfsTer11
ENST00000381583.6:c.752del	ENSP00000370995.2:p.Pro251ArgfsTer11
ENST00000478145.6:n.146del
ENST00000497407.2:n.234del
NM_001039508.1:c.752del	NP_001034597.1:p.Pro251ArgfsTer11
NM_018556.3:c.1085del	NP_061026.2:p.Pro362ArgfsTer11
NM_080816.2:c.434del	NP_543006.2:p.Pro145ArgfsTer11
XM_005260749.2:c.767del	XP_005260806.1:p.Pro256ArgfsTer11
XM_011529286.1:c.986del	XP_011527588.1:p.Pro329ArgfsTer11
XM_005260749.4:c.767del	XP_005260806.1:p.Pro256ArgfsTer11
XM_011529286.2:c.986del	XP_011527588.1:p.Pro329ArgfsTer11
NM_018556.4:c.1085del MANE Select	NP_061026.2:p.Pro362ArgfsTer11
NM_080816.3:c.434del	NP_543006.2:p.Pro145ArgfsTer11
NM_001039508.2:c.752del	NP_001034597.1:p.Pro251ArgfsTer11