Canonical Allele Identifier: CA2804766380
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755300_74755301insAAAAA , CM000677.2:g.74755300_74755301insAAAAA GRCh38
NC_000015.9:g.75047641_75047642insAAAAA , CM000677.1:g.75047641_75047642insAAAAA GRCh37
NC_000015.8:g.72834694_72834695insAAAAA NCBI36
NG_008431.1:g.37759_37760insAAAAA
NG_008431.2:g.37759_37760insAAAAA
NG_061543.1:g.11456_11457insAAAAA

Transcript Alleles

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