Canonical Allele Identifier: CA2667574789
Gene: GP9 HGNC NCBI

Linked Data

gnomAD v4: 3-129061862-C-CGGA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061863_129061865dup , CM000665.2:g.129061863_129061865dup GRCh38
NC_000003.11:g.128780706_128780708dup , CM000665.1:g.128780706_128780708dup GRCh37
NC_000003.10:g.130263396_130263398dup NCBI36
NG_008715.1:g.6062_6064dup , LRG_477:g.6062_6064dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.124_126dup MANE Select ENSP00000303942.4:p.Gly42_Leu43insGly
ENST00000307395.4:c.124_126dup ENSP00000303942.4:p.Gly42_Leu43insGly
NM_000174.4:c.124_126dup , LRG_477t1:c.124_126dup NP_000165.1:p.Gly42_Leu43insGly
XM_005247374.3:c.124_126dup XP_005247431.1:p.Gly42_Leu43insGly
XM_011512701.1:c.124_126dup XP_011511003.1:p.Gly42_Leu43insGly
XM_011512702.1:c.124_126dup XP_011511004.1:p.Gly42_Leu43insGly
NM_000174.5:c.124_126dup MANE Select NP_000165.1:p.Gly42_Leu43insGly
Search 100 bp 5'
Search 100 bp 3'