Canonical Allele Identifier: CA393163847

Gene: CYP1A1

Linked Data

• MyVariant Identifiers: chr15:g.75012894G>T (hg19) ; chr15:g.74720553G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720553G>T , CM000677.2:g.74720553G>T	GRCh38
NC_000015.9:g.75012894G>T , CM000677.1:g.75012894G>T	GRCh37
NC_000015.8:g.72799947G>T	NCBI36
NG_008431.1:g.3012G>T
NG_008431.2:g.3012G>T
NG_061374.1:g.9976C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000379727.8:c.1475C>A MANE Select	ENSP00000369050.3:p.Pro492His
ENST00000379727.7:c.1475C>A	ENSP00000369050.3:p.Pro492His
ENST00000395048.6:c.1475C>A	ENSP00000378488.2:p.Pro492His
ENST00000395049.8:c.1388C>A	ENSP00000378489.4:p.Pro463His
ENST00000567032.5:c.1475C>A	ENSP00000456585.1:p.Pro492His
ENST00000612821.4:c.1391C>A	ENSP00000479744.1:p.Pro464His
ENST00000617691.4:c.1388C>A	ENSP00000482863.1:p.Pro463His
NM_000499.3:c.1475C>A	NP_000490.1:p.Pro492His
XM_005254185.1:c.1475C>A	XP_005254242.1:p.Pro492His
NM_000499.5:c.1475C>A	NP_000490.1:p.Pro492His
NM_001319216.2:c.1388C>A	NP_001306145.1:p.Pro463His
NM_001319217.2:c.1475C>A MANE Select	NP_001306146.1:p.Pro492His