Canonical Allele Identifier: CA2629512239

Gene: CYP1A2

Linked Data

• gnomAD v4: 15-74755380-A-AAAAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755380_74755381insAAAAC , CM000677.2:g.74755380_74755381insAAAAC	GRCh38
NC_000015.9:g.75047721_75047722insAAAAC , CM000677.1:g.75047721_75047722insAAAAC	GRCh37
NC_000015.8:g.72834774_72834775insAAAAC	NCBI36
NG_008431.1:g.37839_37840insAAAAC
NG_008431.2:g.37839_37840insAAAAC
NG_061543.1:g.11536_11537insAAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*292_*293insAAAAC MANE Select	ENSP00000342007.4:n.*292_*293insAAAAC
ENST00000343932.4:c.*292_*293insAAAAC	ENSP00000342007.4:n.*292_*293insAAAAC
NM_000761.4:c.*292_*293insAAAAC	NP_000752.2:n.*292_*293insAAAAC
NM_000761.5:c.*292_*293insAAAAC MANE Select	NP_000752.2:n.*292_*293insAAAAC