Canonical Allele Identifier: CA2187827332

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755370_74755374delinsCAAAA , CM000677.2:g.74755370_74755374delinsCAAAA	GRCh38
NC_000015.9:g.75047711_75047715delinsCAAAA , CM000677.1:g.75047711_75047715delinsCAAAA	GRCh37
NC_000015.8:g.72834764_72834768delinsCAAAA	NCBI36
NG_008431.1:g.37829_37833delinsCAAAA
NG_008431.2:g.37829_37833delinsCAAAA
NG_061543.1:g.11526_11530delinsCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*282_*286delinsCAAAA MANE Select	ENSP00000342007.4:n.*282_*286delinsCAAAA
ENST00000343932.4:c.*282_*286delinsCAAAA	ENSP00000342007.4:n.*282_*286delinsCAAAA
NM_000761.4:c.*282_*286delinsCAAAA	NP_000752.2:n.*282_*286delinsCAAAA
NM_000761.5:c.*282_*286delinsCAAAA MANE Select	NP_000752.2:n.*282_*286delinsCAAAA