Canonical Allele Identifier: CA2187814954
Gene: CYP1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720685A= , CM000677.2:g.74720685A= GRCh38
NC_000015.9:g.75013026A= , CM000677.1:g.75013026A= GRCh37
NC_000015.8:g.72800079A= NCBI36
NG_008431.1:g.3144A=
NG_008431.2:g.3144A=
NG_061374.1:g.9844T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.1343T= MANE Select ENSP00000369050.3:p.Ile448=
ENST00000379727.7:c.1343T= ENSP00000369050.3:p.Ile448=
ENST00000395048.6:c.1343T= ENSP00000378488.2:p.Ile448=
ENST00000395049.8:c.1256T= ENSP00000378489.4:p.Ile419=
ENST00000567032.5:c.1343T= ENSP00000456585.1:p.Ile448=
ENST00000612821.4:c.1259T= ENSP00000479744.1:p.Ile420=
ENST00000617691.4:c.1256T= ENSP00000482863.1:p.Ile419=
NM_000499.3:c.1343T= NP_000490.1:p.Ile448=
XM_005254185.1:c.1343T= XP_005254242.1:p.Ile448=
NM_000499.5:c.1343T= NP_000490.1:p.Ile448=
NM_001319216.2:c.1256T= NP_001306145.1:p.Ile419=
NM_001319217.2:c.1343T= MANE Select NP_001306146.1:p.Ile448=