Canonical Allele Identifier: CA2590786016
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Linked Data

gnomAD v3: 5-437858-T-G
gnomAD v4: 5-437858-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437858T>G , CM000667.2:g.437858T>G GRCh38
NC_000005.9:g.437973T>G , CM000667.1:g.437973T>G GRCh37
NC_000005.8:g.490973T>G NCBI36
NG_029834.1:g.138683T>G
NG_029834.2:g.138683T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684583.1:c.*3024T>G (AHRR) MANE Select ENSP00000507476.1:n.*3024T>G
ENST00000316418.10:c.*3024T>G (AHRR) ENSP00000323816.6:n.*3024T>G
ENST00000505113.6:c.*5114T>G (PDCD6-AHRR) ENSP00000424601.2:n.*5114T>G
ENST00000675395.1:c.*5168T>G (PDCD6-AHRR) ENSP00000502570.1:n.*5168T>G
ENST00000316418.9:c.*3024T>G (AHRR) ENSP00000323816.5:n.*3024T>G
NM_001242412.1:c.*3024T>G (AHRR) NP_001229341.1:n.*3024T>G
NM_020731.4:c.*3024T>G (AHRR) NP_065782.2:n.*3024T>G
NM_001377236.1:c.*3024T>G (AHRR) MANE Select NP_001364165.1:n.*3024T>G
NM_001377239.1:c.*3024T>G (AHRR) NP_001364168.1:n.*3024T>G
NR_165159.2:n.5465T>G (PDCD6-AHRR)
NR_165163.2:n.5411T>G (PDCD6-AHRR)
Search 100 bp 5'
Search 100 bp 3'