Canonical Allele Identifier: CA2667574637
Gene: GP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061579_129061580insGCGGAGAAAGTTGAGCCCATAAAAAACCT , CM000665.2:g.129061579_129061580insGCGGAGAAAGTTGAGCCCATAAAAAACCT GRCh38
NC_000003.11:g.128780422_128780423insGCGGAGAAAGTTGAGCCCATAAAAAACCT , CM000665.1:g.128780422_128780423insGCGGAGAAAGTTGAGCCCATAAAAAACCT GRCh37
NC_000003.10:g.130263112_130263113insGCGGAGAAAGTTGAGCCCATAAAAAACCT NCBI36
NG_008715.1:g.5778_5779insGCGGAGAAAGTTGAGCCCATAAAAAACCT , LRG_477:g.5778_5779insGCGGAGAAAGTTGAGCCCATAAAAAACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT MANE Select ENSP00000303942.4:n.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT
ENST00000307395.4:c.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT ENSP00000303942.4:n.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT
NM_000174.4:c.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT , LRG_477t1:c.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT NP_000165.1:n.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT
XM_005247374.3:c.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT XP_005247431.1:n.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT
XM_011512701.1:c.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT XP_011511003.1:n.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT
XM_011512702.1:c.-12-149_-12-148insGCGGAGAAAGTTGAGCCCATAAAAAACCT XP_011511004.1:n.-12-149_-12-148insGCGGAGAAAGTTGAGCCCATAAAAAA...
NM_000174.5:c.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT MANE Select NP_000165.1:n.-53_-52insGCGGAGAAAGTTGAGCCCATAAAAAACCT