Canonical Allele Identifier: CA2187827267
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755300_74755301delinsAC , CM000677.2:g.74755300_74755301delinsAC GRCh38
NC_000015.9:g.75047641_75047642delinsAC , CM000677.1:g.75047641_75047642delinsAC GRCh37
NC_000015.8:g.72834694_72834695delinsAC NCBI36
NG_008431.1:g.37759_37760delinsAC
NG_008431.2:g.37759_37760delinsAC
NG_061543.1:g.11456_11457delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*212_*213delinsAC MANE Select ENSP00000342007.4:n.*212_*213delinsAC
ENST00000343932.4:c.*212_*213delinsAC ENSP00000342007.4:n.*212_*213delinsAC
NM_000761.4:c.*212_*213delinsAC NP_000752.2:n.*212_*213delinsAC
NM_000761.5:c.*212_*213delinsAC MANE Select NP_000752.2:n.*212_*213delinsAC