Canonical Allele Identifier: CA2629502724
Gene: CYP1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719656G>T , CM000677.2:g.74719656G>T GRCh38
NC_000015.9:g.75011997G>T , CM000677.1:g.75011997G>T GRCh37
NC_000015.8:g.72799050G>T NCBI36
NG_008431.1:g.2115G>T
NG_008431.2:g.2115G>T
NG_061374.1:g.10873C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*833C>A MANE Select ENSP00000369050.3:n.*833C>A
ENST00000379727.7:c.*833C>A ENSP00000369050.3:n.*833C>A
ENST00000395048.6:c.*833C>A ENSP00000378488.2:n.*833C>A
ENST00000612821.4:c.2288C>A ENSP00000479744.1:n.2288C>A
ENST00000617691.4:c.*833C>A ENSP00000482863.1:n.*833C>A
NM_000499.3:c.*833C>A NP_000490.1:n.*833C>A
XM_005254185.1:c.*833C>A XP_005254242.1:n.*833C>A
NM_000499.5:c.*833C>A NP_000490.1:n.*833C>A
NM_001319216.2:c.*833C>A NP_001306145.1:n.*833C>A
NM_001319217.2:c.*833C>A MANE Select NP_001306146.1:n.*833C>A