Canonical Allele Identifier: CA2187827309

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755359_74755362delinsAAAC , CM000677.2:g.74755359_74755362delinsAAAC	GRCh38
NC_000015.9:g.75047700_75047703delinsAAAC , CM000677.1:g.75047700_75047703delinsAAAC	GRCh37
NC_000015.8:g.72834753_72834756delinsAAAC	NCBI36
NG_008431.1:g.37818_37821delinsAAAC
NG_008431.2:g.37818_37821delinsAAAC
NG_061543.1:g.11515_11518delinsAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*271_*274delinsAAAC MANE Select	ENSP00000342007.4:n.*271_*274delinsAAAC
ENST00000343932.4:c.*271_*274delinsAAAC	ENSP00000342007.4:n.*271_*274delinsAAAC
NM_000761.4:c.*271_*274delinsAAAC	NP_000752.2:n.*271_*274delinsAAAC
NM_000761.5:c.*271_*274delinsAAAC MANE Select	NP_000752.2:n.*271_*274delinsAAAC