Canonical Allele Identifier: CA2187827323
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755365_74755370delinsACAAAC , CM000677.2:g.74755365_74755370delinsACAAAC GRCh38
NC_000015.9:g.75047706_75047711delinsACAAAC , CM000677.1:g.75047706_75047711delinsACAAAC GRCh37
NC_000015.8:g.72834759_72834764delinsACAAAC NCBI36
NG_008431.1:g.37824_37829delinsACAAAC
NG_008431.2:g.37824_37829delinsACAAAC
NG_061543.1:g.11521_11526delinsACAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*277_*282delinsACAAAC MANE Select ENSP00000342007.4:n.*277_*282delinsACAAAC
ENST00000343932.4:c.*277_*282delinsACAAAC ENSP00000342007.4:n.*277_*282delinsACAAAC
NM_000761.4:c.*277_*282delinsACAAAC NP_000752.2:n.*277_*282delinsACAAAC
NM_000761.5:c.*277_*282delinsACAAAC MANE Select NP_000752.2:n.*277_*282delinsACAAAC