Canonical Allele Identifier: CA2187827268
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755301_74755302delinsCA , CM000677.2:g.74755301_74755302delinsCA GRCh38
NC_000015.9:g.75047642_75047643delinsCA , CM000677.1:g.75047642_75047643delinsCA GRCh37
NC_000015.8:g.72834695_72834696delinsCA NCBI36
NG_008431.1:g.37760_37761delinsCA
NG_008431.2:g.37760_37761delinsCA
NG_061543.1:g.11457_11458delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*213_*214delinsCA MANE Select ENSP00000342007.4:n.*213_*214delinsCA
ENST00000343932.4:c.*213_*214delinsCA ENSP00000342007.4:n.*213_*214delinsCA
NM_000761.4:c.*213_*214delinsCA NP_000752.2:n.*213_*214delinsCA
NM_000761.5:c.*213_*214delinsCA MANE Select NP_000752.2:n.*213_*214delinsCA