Canonical Allele Identifier: CA393164453
Gene: CYP1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720722C>A , CM000677.2:g.74720722C>A GRCh38
NC_000015.9:g.75013063C>A , CM000677.1:g.75013063C>A GRCh37
NC_000015.8:g.72800116C>A NCBI36
NG_008431.1:g.3181C>A
NG_008431.2:g.3181C>A
NG_061374.1:g.9807G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.1306G>T MANE Select ENSP00000369050.3:p.Asp436Tyr
ENST00000379727.7:c.1306G>T ENSP00000369050.3:p.Asp436Tyr
ENST00000395048.6:c.1306G>T ENSP00000378488.2:p.Asp436Tyr
ENST00000395049.8:c.1219G>T ENSP00000378489.4:p.Asp407Tyr
ENST00000562201.5:c.*543G>T ENSP00000455340.1:n.*543G>T
ENST00000564596.5:c.*241G>T ENSP00000457668.1:n.*241G>T
ENST00000566503.1:c.523G>T ENSP00000455846.1:p.Asp175Tyr
ENST00000567032.5:c.1306G>T ENSP00000456585.1:p.Asp436Tyr
ENST00000569630.5:c.*895G>T ENSP00000455051.1:n.*895G>T
ENST00000612821.4:c.1222G>T ENSP00000479744.1:p.Asp408Tyr
ENST00000617691.4:c.1219G>T ENSP00000482863.1:p.Asp407Tyr
NM_000499.3:c.1306G>T NP_000490.1:p.Asp436Tyr
XM_005254185.1:c.1306G>T XP_005254242.1:p.Asp436Tyr
NM_000499.5:c.1306G>T NP_000490.1:p.Asp436Tyr
NM_001319216.2:c.1219G>T NP_001306145.1:p.Asp407Tyr
NM_001319217.2:c.1306G>T MANE Select NP_001306146.1:p.Asp436Tyr