Canonical Allele Identifier: CA2681909913

Gene: AHR

Linked Data

• gnomAD v4: 7-17339689-C-CTTTTT

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