Canonical Allele Identifier: CA2187827329

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755368_74755370delinsAAC , CM000677.2:g.74755368_74755370delinsAAC	GRCh38
NC_000015.9:g.75047709_75047711delinsAAC , CM000677.1:g.75047709_75047711delinsAAC	GRCh37
NC_000015.8:g.72834762_72834764delinsAAC	NCBI36
NG_008431.1:g.37827_37829delinsAAC
NG_008431.2:g.37827_37829delinsAAC
NG_061543.1:g.11524_11526delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*280_*282delinsAAC MANE Select	ENSP00000342007.4:n.*280_*282delinsAAC
ENST00000343932.4:c.*280_*282delinsAAC	ENSP00000342007.4:n.*280_*282delinsAAC
NM_000761.4:c.*280_*282delinsAAC	NP_000752.2:n.*280_*282delinsAAC
NM_000761.5:c.*280_*282delinsAAC MANE Select	NP_000752.2:n.*280_*282delinsAAC