Canonical Allele Identifier: CA2672992412
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Linked Data

gnomAD v4: 5-437910-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437910A>G , CM000667.2:g.437910A>G GRCh38
NC_000005.9:g.438025A>G , CM000667.1:g.438025A>G GRCh37
NC_000005.8:g.491025A>G NCBI36
NG_029834.1:g.138735A>G
NG_029834.2:g.138735A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684583.1:c.*3076A>G (AHRR) MANE Select ENSP00000507476.1:n.*3076A>G
ENST00000316418.10:c.*3076A>G (AHRR) ENSP00000323816.6:n.*3076A>G
ENST00000505113.6:c.*5166A>G (PDCD6-AHRR) ENSP00000424601.2:n.*5166A>G
ENST00000675395.1:c.*5220A>G (PDCD6-AHRR) ENSP00000502570.1:n.*5220A>G
ENST00000316418.9:c.*3076A>G (AHRR) ENSP00000323816.5:n.*3076A>G
NM_001242412.1:c.*3076A>G (AHRR) NP_001229341.1:n.*3076A>G
NM_020731.4:c.*3076A>G (AHRR) NP_065782.2:n.*3076A>G
NM_001377236.1:c.*3076A>G (AHRR) MANE Select NP_001364165.1:n.*3076A>G
NM_001377239.1:c.*3076A>G (AHRR) NP_001364168.1:n.*3076A>G
NR_165159.2:n.5517A>G (PDCD6-AHRR)
NR_165163.2:n.5463A>G (PDCD6-AHRR)
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