Canonical Allele Identifier: CA1691323951

Gene: AHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339748G= , CM000669.2:g.17339748G=	GRCh38
NC_000007.13:g.17379372G= , CM000669.1:g.17379372G=	GRCh37
NC_000007.12:g.17345897G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1923G= MANE Select	ENSP00000242057.4:p.Lys641=
ENST00000637807.1:c.1893G=	ENSP00000490530.1:p.Lys631=
ENST00000642825.1:c.1878G=	ENSP00000495987.1:p.Lys626=
ENST00000242057.8:c.1923G=	ENSP00000242057.4:p.Lys641=
ENST00000463496.1:c.1923G=	ENSP00000436466.1:p.Lys641=
NM_001621.4:c.1923G=	NP_001612.1:p.Lys641=
NM_001621.5:c.1923G= MANE Select	NP_001612.1:p.Lys641=