Canonical Allele Identifier: CA1522097551
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437995_437996delinsCT , CM000667.2:g.437995_437996delinsCT GRCh38
NC_000005.9:g.438110_438111delinsCT , CM000667.1:g.438110_438111delinsCT GRCh37
NC_000005.8:g.491110_491111delinsCT NCBI36
NG_029834.1:g.138820_138821delinsCT
NG_029834.2:g.138820_138821delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000684583.1:c.*3161_*3162delinsCT (AHRR) MANE Select ENSP00000507476.1:n.*3161_*3162delinsCT
ENST00000316418.10:c.*3161_*3162delinsCT (AHRR) ENSP00000323816.6:n.*3161_*3162delinsCT
ENST00000505113.6:c.*5251_*5252delinsCT (PDCD6-AHRR) ENSP00000424601.2:n.*5251_*5252delinsCT
ENST00000675395.1:c.*5305_*5306delinsCT (PDCD6-AHRR) ENSP00000502570.1:n.*5305_*5306delinsCT
ENST00000316418.9:c.*3161_*3162delinsCT (AHRR) ENSP00000323816.5:n.*3161_*3162delinsCT
NM_001242412.1:c.*3161_*3162delinsCT (AHRR) NP_001229341.1:n.*3161_*3162delinsCT
NM_020731.4:c.*3161_*3162delinsCT (AHRR) NP_065782.2:n.*3161_*3162delinsCT
NM_001377236.1:c.*3161_*3162delinsCT (AHRR) MANE Select NP_001364165.1:n.*3161_*3162delinsCT
NM_001377239.1:c.*3161_*3162delinsCT (AHRR) NP_001364168.1:n.*3161_*3162delinsCT
NR_165159.2:n.5602_5603delinsCT (PDCD6-AHRR)
NR_165163.2:n.5548_5549delinsCT (PDCD6-AHRR)