Canonical Allele Identifier: CA2667574793

Gene: GP9

Linked Data

• gnomAD v4: 3-129061991-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061993del , CM000665.2:g.129061993del	GRCh38
NC_000003.11:g.128780836del , CM000665.1:g.128780836del	GRCh37
NC_000003.10:g.130263526del	NCBI36
NG_008715.1:g.6192del , LRG_477:g.6192del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.254del MANE Select	ENSP00000303942.4:p.Asn85ThrfsTer?
ENST00000307395.4:c.254del	ENSP00000303942.4:p.Asn85ThrfsTer?
NM_000174.4:c.254del , LRG_477t1:c.254del	NP_000165.1:p.Asn85ThrfsTer?
XM_005247374.3:c.254del	XP_005247431.1:p.Asn85ThrfsTer?
XM_011512701.1:c.254del	XP_011511003.1:p.Asn85ThrfsTer?
XM_011512702.1:c.254del	XP_011511004.1:p.Asn85ThrfsTer?
NM_000174.5:c.254del MANE Select	NP_000165.1:p.Asn85ThrfsTer?