Canonical Allele Identifier: CA2629512135
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755300_74755301insAAA , CM000677.2:g.74755300_74755301insAAA GRCh38
NC_000015.9:g.75047641_75047642insAAA , CM000677.1:g.75047641_75047642insAAA GRCh37
NC_000015.8:g.72834694_72834695insAAA NCBI36
NG_008431.1:g.37759_37760insAAA
NG_008431.2:g.37759_37760insAAA
NG_061543.1:g.11456_11457insAAA

Transcript Alleles

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