Canonical Allele Identifier: CA2681909913
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339689-C-CTTTTT
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339689_17339690insTTTTT , CM000669.2:g.17339689_17339690insTTTTT GRCh38
NC_000007.13:g.17379313_17379314insTTTTT , CM000669.1:g.17379313_17379314insTTTTT GRCh37
NC_000007.12:g.17345838_17345839insTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1864_1865insTTTTT MANE Select ENSP00000242057.4:p.Gln622LeufsTer11
ENST00000637807.1:c.1834_1835insTTTTT ENSP00000490530.1:p.Gln612LeufsTer11
ENST00000642825.1:c.1819_1820insTTTTT ENSP00000495987.1:p.Gln607LeufsTer11
ENST00000242057.8:c.1864_1865insTTTTT ENSP00000242057.4:p.Gln622LeufsTer11
ENST00000463496.1:c.1864_1865insTTTTT ENSP00000436466.1:p.Gln622LeufsTer11
NM_001621.4:c.1864_1865insTTTTT NP_001612.1:p.Gln622LeufsTer11
NM_001621.5:c.1864_1865insTTTTT MANE Select NP_001612.1:p.Gln622LeufsTer11
Search 100 bp 5'
Search 100 bp 3'