Canonical Allele Identifier: CA2672992478
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Linked Data

gnomAD v4: 5-438002-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.438002C>A , CM000667.2:g.438002C>A GRCh38
NC_000005.9:g.438117C>A , CM000667.1:g.438117C>A GRCh37
NC_000005.8:g.491117C>A NCBI36
NG_029834.1:g.138827C>A
NG_029834.2:g.138827C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684583.1:c.*3168C>A (AHRR) MANE Select ENSP00000507476.1:n.*3168C>A
ENST00000316418.10:c.*3168C>A (AHRR) ENSP00000323816.6:n.*3168C>A
ENST00000505113.6:c.*5258C>A (PDCD6-AHRR) ENSP00000424601.2:n.*5258C>A
ENST00000675395.1:c.*5312C>A (PDCD6-AHRR) ENSP00000502570.1:n.*5312C>A
ENST00000316418.9:c.*3168C>A (AHRR) ENSP00000323816.5:n.*3168C>A
NM_001242412.1:c.*3168C>A (AHRR) NP_001229341.1:n.*3168C>A
NM_020731.4:c.*3168C>A (AHRR) NP_065782.2:n.*3168C>A
NM_001377236.1:c.*3168C>A (AHRR) MANE Select NP_001364165.1:n.*3168C>A
NM_001377239.1:c.*3168C>A (AHRR) NP_001364168.1:n.*3168C>A
NR_165159.2:n.5609C>A (PDCD6-AHRR)
NR_165163.2:n.5555C>A (PDCD6-AHRR)
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