Canonical Allele Identifier: CA2667574788

Gene: GP9

Linked Data

• gnomAD v4: 3-129061858-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061860del , CM000665.2:g.129061860del	GRCh38
NC_000003.11:g.128780703del , CM000665.1:g.128780703del	GRCh37
NC_000003.10:g.130263393del	NCBI36
NG_008715.1:g.6059del , LRG_477:g.6059del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.121del MANE Select	ENSP00000303942.4:p.His41ThrfsTer?
ENST00000307395.4:c.121del	ENSP00000303942.4:p.His41ThrfsTer?
NM_000174.4:c.121del , LRG_477t1:c.121del	NP_000165.1:p.His41ThrfsTer?
XM_005247374.3:c.121del	XP_005247431.1:p.His41ThrfsTer?
XM_011512701.1:c.121del	XP_011511003.1:p.His41ThrfsTer?
XM_011512702.1:c.121del	XP_011511004.1:p.His41ThrfsTer?
NM_000174.5:c.121del MANE Select	NP_000165.1:p.His41ThrfsTer?