Canonical Allele Identifier: CA1522097466
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Linked Data

dbSNP Id: rs115432082

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437815C>A , CM000667.2:g.437815C>A GRCh38
NC_000005.9:g.437930C>A , CM000667.1:g.437930C>A GRCh37
NC_000005.8:g.490930C>A NCBI36
NG_029834.1:g.138640C>A
NG_029834.2:g.138640C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684583.1:c.*2981C>A (AHRR) MANE Select ENSP00000507476.1:n.*2981C>A
ENST00000316418.10:c.*2981C>A (AHRR) ENSP00000323816.6:n.*2981C>A
ENST00000505113.6:c.*5071C>A (PDCD6-AHRR) ENSP00000424601.2:n.*5071C>A
ENST00000675395.1:c.*5125C>A (PDCD6-AHRR) ENSP00000502570.1:n.*5125C>A
ENST00000316418.9:c.*2981C>A (AHRR) ENSP00000323816.5:n.*2981C>A
NM_001242412.1:c.*2981C>A (AHRR) NP_001229341.1:n.*2981C>A
NM_020731.4:c.*2981C>A (AHRR) NP_065782.2:n.*2981C>A
NM_001377236.1:c.*2981C>A (AHRR) MANE Select NP_001364165.1:n.*2981C>A
NM_001377239.1:c.*2981C>A (AHRR) NP_001364168.1:n.*2981C>A
NR_165159.2:n.5422C>A (PDCD6-AHRR)
NR_165163.2:n.5368C>A (PDCD6-AHRR)