Canonical Allele Identifier: CA2629502711
Gene: CYP1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719597del , CM000677.2:g.74719597del GRCh38
NC_000015.9:g.75011938del , CM000677.1:g.75011938del GRCh37
NC_000015.8:g.72798991del NCBI36
NG_008431.1:g.2056del
NG_008431.2:g.2056del
NG_061374.1:g.10936del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*896del MANE Select ENSP00000369050.3:n.*896del
ENST00000379727.7:c.*896del ENSP00000369050.3:n.*896del
ENST00000395048.6:c.*896del ENSP00000378488.2:n.*896del
ENST00000612821.4:c.2351del ENSP00000479744.1:n.2351del
ENST00000617691.4:c.*896del ENSP00000482863.1:n.*896del
NM_000499.3:c.*896del NP_000490.1:n.*896del
XM_005254185.1:c.*896del XP_005254242.1:n.*896del
NM_000499.5:c.*896del NP_000490.1:n.*896del
NM_001319216.2:c.*896del NP_001306145.1:n.*896del
NM_001319217.2:c.*896del MANE Select NP_001306146.1:n.*896del