Canonical Allele Identifier: CA272812639
Gene: CYP1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1048943

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720644T>A , CM000677.2:g.74720644T>A GRCh38
NC_000015.9:g.75012985T>A , CM000677.1:g.75012985T>A GRCh37
NC_000015.8:g.72800038T>A NCBI36
NG_008431.1:g.3103T>A
NG_008431.2:g.3103T>A
NG_061374.1:g.9885A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379727.8:c.1384A>T MANE Select ENSP00000369050.3:p.Ile462Phe
ENST00000379727.7:c.1384A>T ENSP00000369050.3:p.Ile462Phe
ENST00000395048.6:c.1384A>T ENSP00000378488.2:p.Ile462Phe
ENST00000395049.8:c.1297A>T ENSP00000378489.4:p.Ile433Phe
ENST00000567032.5:c.1384A>T ENSP00000456585.1:p.Ile462Phe
ENST00000612821.4:c.1300A>T ENSP00000479744.1:p.Ile434Phe
ENST00000617691.4:c.1297A>T ENSP00000482863.1:p.Ile433Phe
NM_000499.3:c.1384A>T NP_000490.1:p.Ile462Phe
XM_005254185.1:c.1384A>T XP_005254242.1:p.Ile462Phe
NM_000499.5:c.1384A>T NP_000490.1:p.Ile462Phe
NM_001319216.2:c.1297A>T NP_001306145.1:p.Ile433Phe
NM_001319217.2:c.1384A>T MANE Select NP_001306146.1:p.Ile462Phe