Canonical Allele Identifier: CA2575790090
Gene: CYP1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720571dup , CM000677.2:g.74720571dup GRCh38
NC_000015.9:g.75012912dup , CM000677.1:g.75012912dup GRCh37
NC_000015.8:g.72799965dup NCBI36
NG_008431.1:g.3030dup
NG_008431.2:g.3030dup
NG_061374.1:g.9958dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.1457dup MANE Select ENSP00000369050.3:p.Lys487GlufsTer18
ENST00000379727.7:c.1457dup ENSP00000369050.3:p.Lys487GlufsTer18
ENST00000395048.6:c.1457dup ENSP00000378488.2:p.Lys487GlufsTer18
ENST00000395049.8:c.1370dup ENSP00000378489.4:p.Lys458GlufsTer18
ENST00000567032.5:c.1457dup ENSP00000456585.1:p.Lys487GlufsTer18
ENST00000612821.4:c.1373dup ENSP00000479744.1:p.Lys459GlufsTer18
ENST00000617691.4:c.1370dup ENSP00000482863.1:p.Lys458GlufsTer18
NM_000499.3:c.1457dup NP_000490.1:p.Lys487GlufsTer18
XM_005254185.1:c.1457dup XP_005254242.1:p.Lys487GlufsTer18
NM_000499.5:c.1457dup NP_000490.1:p.Lys487GlufsTer18
NM_001319216.2:c.1370dup NP_001306145.1:p.Lys458GlufsTer18
NM_001319217.2:c.1457dup MANE Select NP_001306146.1:p.Lys487GlufsTer18