Canonical Allele Identifier: CA2629502852
Gene: CYP1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719748del , CM000677.2:g.74719748del GRCh38
NC_000015.9:g.75012089del , CM000677.1:g.75012089del GRCh37
NC_000015.8:g.72799142del NCBI36
NG_008431.1:g.2207del
NG_008431.2:g.2207del
NG_061374.1:g.10783del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*743del MANE Select ENSP00000369050.3:n.*743del
ENST00000379727.7:c.*743del ENSP00000369050.3:n.*743del
ENST00000395048.6:c.*743del ENSP00000378488.2:n.*743del
ENST00000612821.4:c.2198del ENSP00000479744.1:n.2198del
ENST00000617691.4:c.*743del ENSP00000482863.1:n.*743del
NM_000499.3:c.*743del NP_000490.1:n.*743del
XM_005254185.1:c.*743del XP_005254242.1:n.*743del
NM_000499.5:c.*743del NP_000490.1:n.*743del
NM_001319216.2:c.*743del NP_001306145.1:n.*743del
NM_001319217.2:c.*743del MANE Select NP_001306146.1:n.*743del