Canonical Allele Identifier: CA2667574791
Gene: GP9 HGNC NCBI

Linked Data

gnomAD v4: 3-129061880-T-TGCCCTGCCG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061885_129061893dup , CM000665.2:g.129061885_129061893dup GRCh38
NC_000003.11:g.128780728_128780736dup , CM000665.1:g.128780728_128780736dup GRCh37
NC_000003.10:g.130263418_130263426dup NCBI36
NG_008715.1:g.6084_6092dup , LRG_477:g.6084_6092dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.146_154dup MANE Select ENSP00000303942.4:p.Ala51_Arg52insLeuProAla
ENST00000307395.4:c.146_154dup ENSP00000303942.4:p.Ala51_Arg52insLeuProAla
NM_000174.4:c.146_154dup , LRG_477t1:c.146_154dup NP_000165.1:p.Ala51_Arg52insLeuProAla
XM_005247374.3:c.146_154dup XP_005247431.1:p.Ala51_Arg52insLeuProAla
XM_011512701.1:c.146_154dup XP_011511003.1:p.Ala51_Arg52insLeuProAla
XM_011512702.1:c.146_154dup XP_011511004.1:p.Ala51_Arg52insLeuProAla
NM_000174.5:c.146_154dup MANE Select NP_000165.1:p.Ala51_Arg52insLeuProAla
Search 100 bp 5'
Search 100 bp 3'