Canonical Allele Identifier: CA2667574591
Gene: GP9 HGNC NCBI

Linked Data

gnomAD v4: 3-129061531-CAGTT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061534_129061537del , CM000665.2:g.129061534_129061537del GRCh38
NC_000003.11:g.128780377_128780380del , CM000665.1:g.128780377_128780380del GRCh37
NC_000003.10:g.130263067_130263070del NCBI36
NG_008715.1:g.5733_5736del , LRG_477:g.5733_5736del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-98_-95del MANE Select ENSP00000303942.4:n.-98_-95del
ENST00000307395.4:c.-98_-95del ENSP00000303942.4:n.-98_-95del
NM_000174.4:c.-98_-95del , LRG_477t1:c.-98_-95del NP_000165.1:n.-98_-95del
XM_005247374.3:c.-98_-95del XP_005247431.1:n.-98_-95del
XM_011512701.1:c.-98_-95del XP_011511003.1:n.-98_-95del
XM_011512702.1:c.-12-194_-12-191del XP_011511004.1:n.-12-194_-12-191del
NM_000174.5:c.-98_-95del MANE Select NP_000165.1:n.-98_-95del
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