Canonical Allele Identifier: CA2187814914

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720605_74720611delinsGCAGGAT , CM000677.2:g.74720605_74720611delinsGCAGGAT	GRCh38
NC_000015.9:g.75012946_75012952delinsGCAGGAT , CM000677.1:g.75012946_75012952delinsGCAGGAT	GRCh37
NC_000015.8:g.72799999_72800005delinsGCAGGAT	NCBI36
NG_008431.1:g.3064_3070delinsGCAGGAT
NG_008431.2:g.3064_3070delinsGCAGGAT
NG_061374.1:g.9918_9924delinsATCCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1417_1423delinsATCCTGC MANE Select	ENSP00000369050.3:p.Ile473=
ENST00000379727.7:c.1417_1423delinsATCCTGC	ENSP00000369050.3:p.Ile473=
ENST00000395048.6:c.1417_1423delinsATCCTGC	ENSP00000378488.2:p.Ile473=
ENST00000395049.8:c.1330_1336delinsATCCTGC	ENSP00000378489.4:p.Ile444=
ENST00000567032.5:c.1417_1423delinsATCCTGC	ENSP00000456585.1:p.Ile473=
ENST00000612821.4:c.1333_1339delinsATCCTGC	ENSP00000479744.1:p.Ile445=
ENST00000617691.4:c.1330_1336delinsATCCTGC	ENSP00000482863.1:p.Ile444=
NM_000499.3:c.1417_1423delinsATCCTGC	NP_000490.1:p.Ile473=
XM_005254185.1:c.1417_1423delinsATCCTGC	XP_005254242.1:p.Ile473=
NM_000499.5:c.1417_1423delinsATCCTGC	NP_000490.1:p.Ile473=
NM_001319216.2:c.1330_1336delinsATCCTGC	NP_001306145.1:p.Ile444=
NM_001319217.2:c.1417_1423delinsATCCTGC MANE Select	NP_001306146.1:p.Ile473=