Canonical Allele Identifier: CA393164053
Gene: CYP1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1411228732

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720610A>G , CM000677.2:g.74720610A>G GRCh38
NC_000015.9:g.75012951A>G , CM000677.1:g.75012951A>G GRCh37
NC_000015.8:g.72800004A>G NCBI36
NG_008431.1:g.3069A>G
NG_008431.2:g.3069A>G
NG_061374.1:g.9919T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.1418T>C MANE Select ENSP00000369050.3:p.Ile473Thr
ENST00000379727.7:c.1418T>C ENSP00000369050.3:p.Ile473Thr
ENST00000395048.6:c.1418T>C ENSP00000378488.2:p.Ile473Thr
ENST00000395049.8:c.1331T>C ENSP00000378489.4:p.Ile444Thr
ENST00000567032.5:c.1418T>C ENSP00000456585.1:p.Ile473Thr
ENST00000612821.4:c.1334T>C ENSP00000479744.1:p.Ile445Thr
ENST00000617691.4:c.1331T>C ENSP00000482863.1:p.Ile444Thr
NM_000499.3:c.1418T>C NP_000490.1:p.Ile473Thr
XM_005254185.1:c.1418T>C XP_005254242.1:p.Ile473Thr
NM_000499.5:c.1418T>C NP_000490.1:p.Ile473Thr
NM_001319216.2:c.1331T>C NP_001306145.1:p.Ile444Thr
NM_001319217.2:c.1418T>C MANE Select NP_001306146.1:p.Ile473Thr