Canonical Allele Identifier: CA2681909917
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339779-G-GA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339783dup , CM000669.2:g.17339783dup GRCh38
NC_000007.13:g.17379407dup , CM000669.1:g.17379407dup GRCh37
NC_000007.12:g.17345932dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1958dup MANE Select ENSP00000242057.4:p.Asn653LysfsTer5
ENST00000637807.1:c.1928dup ENSP00000490530.1:p.Asn643LysfsTer5
ENST00000642825.1:c.1913dup ENSP00000495987.1:p.Asn638LysfsTer5
ENST00000242057.8:c.1958dup ENSP00000242057.4:p.Asn653LysfsTer5
ENST00000463496.1:c.1958dup ENSP00000436466.1:p.Asn653LysfsTer5
NM_001621.4:c.1958dup NP_001612.1:p.Asn653LysfsTer5
NM_001621.5:c.1958dup MANE Select NP_001612.1:p.Asn653LysfsTer5
Search 100 bp 5'
Search 100 bp 3'