Canonical Allele Identifier: CA2187814834

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720452_74720453delinsAG , CM000677.2:g.74720452_74720453delinsAG	GRCh38
NC_000015.9:g.75012793_75012794delinsAG , CM000677.1:g.75012793_75012794delinsAG	GRCh37
NC_000015.8:g.72799846_72799847delinsAG	NCBI36
NG_008431.1:g.2911_2912delinsAG
NG_008431.2:g.2911_2912delinsAG
NG_061374.1:g.10076_10077delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*36_*37delinsCT MANE Select	ENSP00000369050.3:n.*36_*37delinsCT
ENST00000379727.7:c.*36_*37delinsCT	ENSP00000369050.3:n.*36_*37delinsCT
ENST00000395048.6:c.*36_*37delinsCT	ENSP00000378488.2:n.*36_*37delinsCT
ENST00000395049.8:c.*36_*37delinsCT	ENSP00000378489.4:n.*36_*37delinsCT
ENST00000567032.5:c.*36_*37delinsCT	ENSP00000456585.1:n.*36_*37delinsCT
ENST00000612821.4:c.1491_1492delinsCT	ENSP00000479744.1:n.1491_1492delinsCT
ENST00000617691.4:c.*36_*37delinsCT	ENSP00000482863.1:n.*36_*37delinsCT
NM_000499.3:c.*36_*37delinsCT	NP_000490.1:n.*36_*37delinsCT
XM_005254185.1:c.*36_*37delinsCT	XP_005254242.1:n.*36_*37delinsCT
NM_000499.5:c.*36_*37delinsCT	NP_000490.1:n.*36_*37delinsCT
NM_001319216.2:c.*36_*37delinsCT	NP_001306145.1:n.*36_*37delinsCT
NM_001319217.2:c.*36_*37delinsCT MANE Select	NP_001306146.1:n.*36_*37delinsCT