Canonical Allele Identifier: CA2672992356
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Linked Data

gnomAD v4: 5-437854-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437854C>T , CM000667.2:g.437854C>T GRCh38
NC_000005.9:g.437969C>T , CM000667.1:g.437969C>T GRCh37
NC_000005.8:g.490969C>T NCBI36
NG_029834.1:g.138679C>T
NG_029834.2:g.138679C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684583.1:c.*3020C>T (AHRR) MANE Select ENSP00000507476.1:n.*3020C>T
ENST00000316418.10:c.*3020C>T (AHRR) ENSP00000323816.6:n.*3020C>T
ENST00000505113.6:c.*5110C>T (PDCD6-AHRR) ENSP00000424601.2:n.*5110C>T
ENST00000675395.1:c.*5164C>T (PDCD6-AHRR) ENSP00000502570.1:n.*5164C>T
ENST00000316418.9:c.*3020C>T (AHRR) ENSP00000323816.5:n.*3020C>T
NM_001242412.1:c.*3020C>T (AHRR) NP_001229341.1:n.*3020C>T
NM_020731.4:c.*3020C>T (AHRR) NP_065782.2:n.*3020C>T
NM_001377236.1:c.*3020C>T (AHRR) MANE Select NP_001364165.1:n.*3020C>T
NM_001377239.1:c.*3020C>T (AHRR) NP_001364168.1:n.*3020C>T
NR_165159.2:n.5461C>T (PDCD6-AHRR)
NR_165163.2:n.5407C>T (PDCD6-AHRR)