Canonical Allele Identifier: CA1072388314
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Linked Data

dbSNP Id: rs1737168181
gnomAD v3: 5-437995-CT-C
gnomAD v4: 5-437995-CT-C

Genomic Alleles

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

Transcript Alleles

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