Canonical Allele Identifier: CA2765008913
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437968_437972del , CM000667.2:g.437968_437972del GRCh38
NC_000005.9:g.438083_438087del , CM000667.1:g.438083_438087del GRCh37
NC_000005.8:g.491083_491087del NCBI36
NG_029834.1:g.138793_138797del
NG_029834.2:g.138793_138797del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684583.1:c.*3134_*3138del (AHRR) MANE Select ENSP00000507476.1:n.*3134_*3138del
ENST00000316418.10:c.*3134_*3138del (AHRR) ENSP00000323816.6:n.*3134_*3138del
ENST00000505113.6:c.*5224_*5228del (PDCD6-AHRR) ENSP00000424601.2:n.*5224_*5228del
ENST00000675395.1:c.*5278_*5282del (PDCD6-AHRR) ENSP00000502570.1:n.*5278_*5282del
ENST00000316418.9:c.*3134_*3138del (AHRR) ENSP00000323816.5:n.*3134_*3138del
NM_001242412.1:c.*3134_*3138del (AHRR) NP_001229341.1:n.*3134_*3138del
NM_020731.4:c.*3134_*3138del (AHRR) NP_065782.2:n.*3134_*3138del
NM_001377236.1:c.*3134_*3138del (AHRR) MANE Select NP_001364165.1:n.*3134_*3138del
NM_001377239.1:c.*3134_*3138del (AHRR) NP_001364168.1:n.*3134_*3138del
NR_165159.2:n.5575_5579del (PDCD6-AHRR)
NR_165163.2:n.5521_5525del (PDCD6-AHRR)