Canonical Allele Identifier: CA2187827328

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755367_74755370delinsAAAC , CM000677.2:g.74755367_74755370delinsAAAC	GRCh38
NC_000015.9:g.75047708_75047711delinsAAAC , CM000677.1:g.75047708_75047711delinsAAAC	GRCh37
NC_000015.8:g.72834761_72834764delinsAAAC	NCBI36
NG_008431.1:g.37826_37829delinsAAAC
NG_008431.2:g.37826_37829delinsAAAC
NG_061543.1:g.11523_11526delinsAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*279_*282delinsAAAC MANE Select	ENSP00000342007.4:n.*279_*282delinsAAAC
ENST00000343932.4:c.*279_*282delinsAAAC	ENSP00000342007.4:n.*279_*282delinsAAAC
NM_000761.4:c.*279_*282delinsAAAC	NP_000752.2:n.*279_*282delinsAAAC
NM_000761.5:c.*279_*282delinsAAAC MANE Select	NP_000752.2:n.*279_*282delinsAAAC