Canonical Allele Identifier: CA2187814904

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720595_74720596delinsAC , CM000677.2:g.74720595_74720596delinsAC	GRCh38
NC_000015.9:g.75012936_75012937delinsAC , CM000677.1:g.75012936_75012937delinsAC	GRCh37
NC_000015.8:g.72799989_72799990delinsAC	NCBI36
NG_008431.1:g.3054_3055delinsAC
NG_008431.2:g.3054_3055delinsAC
NG_061374.1:g.9933_9934delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1432_1433delinsGT MANE Select	ENSP00000369050.3:p.Val478=
ENST00000379727.7:c.1432_1433delinsGT	ENSP00000369050.3:p.Val478=
ENST00000395048.6:c.1432_1433delinsGT	ENSP00000378488.2:p.Val478=
ENST00000395049.8:c.1345_1346delinsGT	ENSP00000378489.4:p.Val449=
ENST00000567032.5:c.1432_1433delinsGT	ENSP00000456585.1:p.Val478=
ENST00000612821.4:c.1348_1349delinsGT	ENSP00000479744.1:p.Val450=
ENST00000617691.4:c.1345_1346delinsGT	ENSP00000482863.1:p.Val449=
NM_000499.3:c.1432_1433delinsGT	NP_000490.1:p.Val478=
XM_005254185.1:c.1432_1433delinsGT	XP_005254242.1:p.Val478=
NM_000499.5:c.1432_1433delinsGT	NP_000490.1:p.Val478=
NM_001319216.2:c.1345_1346delinsGT	NP_001306145.1:p.Val449=
NM_001319217.2:c.1432_1433delinsGT MANE Select	NP_001306146.1:p.Val478=