Canonical Allele Identifier: CA2681909919

Gene: AHR

Linked Data

• gnomAD v4: 7-17339843-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339844del , CM000669.2:g.17339844del	GRCh38
NC_000007.13:g.17379468del , CM000669.1:g.17379468del	GRCh37
NC_000007.12:g.17345993del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.2019del MANE Select	ENSP00000242057.4:p.Asn673LysfsTer?
ENST00000637807.1:c.1989del	ENSP00000490530.1:p.Asn663LysfsTer?
ENST00000642825.1:c.1974del	ENSP00000495987.1:p.Asn658LysfsTer?
ENST00000242057.8:c.2019del	ENSP00000242057.4:p.Asn673LysfsTer?
ENST00000463496.1:c.2019del	ENSP00000436466.1:p.Asn673LysfsTer?
NM_001621.4:c.2019del	NP_001612.1:p.Asn673LysfsTer?
NM_001621.5:c.2019del MANE Select	NP_001612.1:p.Asn673LysfsTer?