Canonical Allele Identifier: CA1691323843

Gene: AHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339473T= , CM000669.2:g.17339473T=	GRCh38
NC_000007.13:g.17379097T= , CM000669.1:g.17379097T=	GRCh37
NC_000007.12:g.17345622T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1648T= MANE Select	ENSP00000242057.4:p.Phe550=
ENST00000637807.1:c.1618T=	ENSP00000490530.1:p.Phe540=
ENST00000642825.1:c.1603T=	ENSP00000495987.1:p.Phe535=
ENST00000242057.8:c.1648T=	ENSP00000242057.4:p.Phe550=
ENST00000463496.1:c.1648T=	ENSP00000436466.1:p.Phe550=
ENST00000492120.1:n.630T=
NM_001621.4:c.1648T=	NP_001612.1:p.Phe550=
NM_001621.5:c.1648T= MANE Select	NP_001612.1:p.Phe550=