Canonical Allele Identifier: CA2187825688

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74752092_74752094delinsCCT , CM000677.2:g.74752092_74752094delinsCCT	GRCh38
NC_000015.9:g.75044433_75044435delinsCCT , CM000677.1:g.75044433_75044435delinsCCT	GRCh37
NC_000015.8:g.72831486_72831488delinsCCT	NCBI36
NG_008431.1:g.34551_34553delinsCCT
NG_008431.2:g.34551_34553delinsCCT
NG_061543.1:g.8248_8250delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1043-32_1043-30delinsCCT MANE Select	ENSP00000342007.4:n.1043-32_1043-30delinsCCT
ENST00000343932.4:c.1043-32_1043-30delinsCCT	ENSP00000342007.4:n.1043-32_1043-30delinsCCT
NM_000761.4:c.1043-32_1043-30delinsCCT	NP_000752.2:n.1043-32_1043-30delinsCCT
NM_000761.5:c.1043-32_1043-30delinsCCT MANE Select	NP_000752.2:n.1043-32_1043-30delinsCCT