Canonical Allele Identifier: CA393163998

Gene: CYP1A1

Linked Data

• MyVariant Identifiers: chr15:g.75012936A>T (hg19) ; chr15:g.74720595A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720595A>T , CM000677.2:g.74720595A>T	GRCh38
NC_000015.9:g.75012936A>T , CM000677.1:g.75012936A>T	GRCh37
NC_000015.8:g.72799989A>T	NCBI36
NG_008431.1:g.3054A>T
NG_008431.2:g.3054A>T
NG_061374.1:g.9934T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1433T>A MANE Select	ENSP00000369050.3:p.Val478Glu
ENST00000379727.7:c.1433T>A	ENSP00000369050.3:p.Val478Glu
ENST00000395048.6:c.1433T>A	ENSP00000378488.2:p.Val478Glu
ENST00000395049.8:c.1346T>A	ENSP00000378489.4:p.Val449Glu
ENST00000567032.5:c.1433T>A	ENSP00000456585.1:p.Val478Glu
ENST00000612821.4:c.1349T>A	ENSP00000479744.1:p.Val450Glu
ENST00000617691.4:c.1346T>A	ENSP00000482863.1:p.Val449Glu
NM_000499.3:c.1433T>A	NP_000490.1:p.Val478Glu
XM_005254185.1:c.1433T>A	XP_005254242.1:p.Val478Glu
NM_000499.5:c.1433T>A	NP_000490.1:p.Val478Glu
NM_001319216.2:c.1346T>A	NP_001306145.1:p.Val449Glu
NM_001319217.2:c.1433T>A MANE Select	NP_001306146.1:p.Val478Glu