Canonical Allele Identifier: CA2629505690
Gene: CYP1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720404_74720417del , CM000677.2:g.74720404_74720417del GRCh38
NC_000015.9:g.75012745_75012758del , CM000677.1:g.75012745_75012758del GRCh37
NC_000015.8:g.72799798_72799811del NCBI36
NG_008431.1:g.2863_2876del
NG_008431.2:g.2863_2876del
NG_061374.1:g.10113_10126del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*73_*86del MANE Select ENSP00000369050.3:n.*73_*86del
ENST00000379727.7:c.*73_*86del ENSP00000369050.3:n.*73_*86del
ENST00000395048.6:c.*73_*86del ENSP00000378488.2:n.*73_*86del
ENST00000567032.5:c.*73_*86del ENSP00000456585.1:n.*73_*86del
ENST00000612821.4:c.1528_1541del ENSP00000479744.1:n.1528_1541del
ENST00000617691.4:c.*73_*86del ENSP00000482863.1:n.*73_*86del
NM_000499.3:c.*73_*86del NP_000490.1:n.*73_*86del
XM_005254185.1:c.*73_*86del XP_005254242.1:n.*73_*86del
NM_000499.5:c.*73_*86del NP_000490.1:n.*73_*86del
NM_001319216.2:c.*73_*86del NP_001306145.1:n.*73_*86del
NM_001319217.2:c.*73_*86del MANE Select NP_001306146.1:n.*73_*86del