Canonical Allele Identifier: CA2765008919
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437999_438003del , CM000667.2:g.437999_438003del GRCh38
NC_000005.9:g.438114_438118del , CM000667.1:g.438114_438118del GRCh37
NC_000005.8:g.491114_491118del NCBI36
NG_029834.1:g.138824_138828del
NG_029834.2:g.138824_138828del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684583.1:c.*3165_*3169del (AHRR) MANE Select ENSP00000507476.1:n.*3165_*3169del
ENST00000316418.10:c.*3165_*3169del (AHRR) ENSP00000323816.6:n.*3165_*3169del
ENST00000505113.6:c.*5255_*5259del (PDCD6-AHRR) ENSP00000424601.2:n.*5255_*5259del
ENST00000675395.1:c.*5309_*5313del (PDCD6-AHRR) ENSP00000502570.1:n.*5309_*5313del
ENST00000316418.9:c.*3165_*3169del (AHRR) ENSP00000323816.5:n.*3165_*3169del
NM_001242412.1:c.*3165_*3169del (AHRR) NP_001229341.1:n.*3165_*3169del
NM_020731.4:c.*3165_*3169del (AHRR) NP_065782.2:n.*3165_*3169del
NM_001377236.1:c.*3165_*3169del (AHRR) MANE Select NP_001364165.1:n.*3165_*3169del
NM_001377239.1:c.*3165_*3169del (AHRR) NP_001364168.1:n.*3165_*3169del
NR_165159.2:n.5606_5610del (PDCD6-AHRR)
NR_165163.2:n.5552_5556del (PDCD6-AHRR)
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