Canonical Allele Identifier: CA2575790090

Gene: CYP1A1

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