Canonical Allele Identifier: CA2629512207

Gene: CYP1A2

Linked Data

• gnomAD v4: 15-74755349-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755349_74755350insAA , CM000677.2:g.74755349_74755350insAA	GRCh38
NC_000015.9:g.75047690_75047691insAA , CM000677.1:g.75047690_75047691insAA	GRCh37
NC_000015.8:g.72834743_72834744insAA	NCBI36
NG_008431.1:g.37808_37809insAA
NG_008431.2:g.37808_37809insAA
NG_061543.1:g.11505_11506insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*261_*262insAA MANE Select	ENSP00000342007.4:n.*261_*262insAA
ENST00000343932.4:c.*261_*262insAA	ENSP00000342007.4:n.*261_*262insAA
NM_000761.4:c.*261_*262insAA	NP_000752.2:n.*261_*262insAA
NM_000761.5:c.*261_*262insAA MANE Select	NP_000752.2:n.*261_*262insAA