Canonical Allele Identifier: CA2629512230

Gene: CYP1A2

Linked Data

• gnomAD v4: 15-74755370-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755370_74755371insCA , CM000677.2:g.74755370_74755371insCA	GRCh38
NC_000015.9:g.75047711_75047712insCA , CM000677.1:g.75047711_75047712insCA	GRCh37
NC_000015.8:g.72834764_72834765insCA	NCBI36
NG_008431.1:g.37829_37830insCA
NG_008431.2:g.37829_37830insCA
NG_061543.1:g.11526_11527insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*282_*283insCA MANE Select	ENSP00000342007.4:n.*282_*283insCA
ENST00000343932.4:c.*282_*283insCA	ENSP00000342007.4:n.*282_*283insCA
NM_000761.4:c.*282_*283insCA	NP_000752.2:n.*282_*283insCA
NM_000761.5:c.*282_*283insCA MANE Select	NP_000752.2:n.*282_*283insCA