Canonical Allele Identifier: CA2187827347
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755380_74755381delinsAC , CM000677.2:g.74755380_74755381delinsAC GRCh38
NC_000015.9:g.75047721_75047722delinsAC , CM000677.1:g.75047721_75047722delinsAC GRCh37
NC_000015.8:g.72834774_72834775delinsAC NCBI36
NG_008431.1:g.37839_37840delinsAC
NG_008431.2:g.37839_37840delinsAC
NG_061543.1:g.11536_11537delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*292_*293delinsAC MANE Select ENSP00000342007.4:n.*292_*293delinsAC
ENST00000343932.4:c.*292_*293delinsAC ENSP00000342007.4:n.*292_*293delinsAC
NM_000761.4:c.*292_*293delinsAC NP_000752.2:n.*292_*293delinsAC
NM_000761.5:c.*292_*293delinsAC MANE Select NP_000752.2:n.*292_*293delinsAC