Canonical Allele Identifier: CA1691323918

Gene: AHR

Linked Data

• dbSNP Id: rs1782397242

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339653dup , CM000669.2:g.17339653dup	GRCh38
NC_000007.13:g.17379277dup , CM000669.1:g.17379277dup	GRCh37
NC_000007.12:g.17345802dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1828dup MANE Select	ENSP00000242057.4:p.Ser610LysfsTer?
ENST00000637807.1:c.1798dup	ENSP00000490530.1:p.Ser600LysfsTer?
ENST00000642825.1:c.1783dup	ENSP00000495987.1:p.Ser595LysfsTer?
ENST00000242057.8:c.1828dup	ENSP00000242057.4:p.Ser610LysfsTer?
ENST00000463496.1:c.1828dup	ENSP00000436466.1:p.Ser610LysfsTer?
NM_001621.4:c.1828dup	NP_001612.1:p.Ser610LysfsTer?
NM_001621.5:c.1828dup MANE Select	NP_001612.1:p.Ser610LysfsTer?