Canonical Allele Identifier: CA2187814939
Gene: CYP1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720653C= , CM000677.2:g.74720653C= GRCh38
NC_000015.9:g.75012994C= , CM000677.1:g.75012994C= GRCh37
NC_000015.8:g.72800047C= NCBI36
NG_008431.1:g.3112C=
NG_008431.2:g.3112C=
NG_061374.1:g.9876G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379727.8:c.1375G= MANE Select ENSP00000369050.3:p.Gly459=
ENST00000379727.7:c.1375G= ENSP00000369050.3:p.Gly459=
ENST00000395048.6:c.1375G= ENSP00000378488.2:p.Gly459=
ENST00000395049.8:c.1288G= ENSP00000378489.4:p.Gly430=
ENST00000567032.5:c.1375G= ENSP00000456585.1:p.Gly459=
ENST00000612821.4:c.1291G= ENSP00000479744.1:p.Gly431=
ENST00000617691.4:c.1288G= ENSP00000482863.1:p.Gly430=
NM_000499.3:c.1375G= NP_000490.1:p.Gly459=
XM_005254185.1:c.1375G= XP_005254242.1:p.Gly459=
NM_000499.5:c.1375G= NP_000490.1:p.Gly459=
NM_001319216.2:c.1288G= NP_001306145.1:p.Gly430=
NM_001319217.2:c.1375G= MANE Select NP_001306146.1:p.Gly459=