Canonical Allele Identifier: CA2187814888

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720561_74720568delinsGTCCACCT , CM000677.2:g.74720561_74720568delinsGTCCACCT	GRCh38
NC_000015.9:g.75012902_75012909delinsGTCCACCT , CM000677.1:g.75012902_75012909delinsGTCCACCT	GRCh37
NC_000015.8:g.72799955_72799962delinsGTCCACCT	NCBI36
NG_008431.1:g.3020_3027delinsGTCCACCT
NG_008431.2:g.3020_3027delinsGTCCACCT
NG_061374.1:g.9961_9968delinsAGGTGGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1460_1467delinsAGGTGGAC MANE Select	ENSP00000369050.3:p.Lys487=
ENST00000379727.7:c.1460_1467delinsAGGTGGAC	ENSP00000369050.3:p.Lys487=
ENST00000395048.6:c.1460_1467delinsAGGTGGAC	ENSP00000378488.2:p.Lys487=
ENST00000395049.8:c.1373_1380delinsAGGTGGAC	ENSP00000378489.4:p.Lys458=
ENST00000567032.5:c.1460_1467delinsAGGTGGAC	ENSP00000456585.1:p.Lys487=
ENST00000612821.4:c.1376_1383delinsAGGTGGAC	ENSP00000479744.1:p.Lys459=
ENST00000617691.4:c.1373_1380delinsAGGTGGAC	ENSP00000482863.1:p.Lys458=
NM_000499.3:c.1460_1467delinsAGGTGGAC	NP_000490.1:p.Lys487=
XM_005254185.1:c.1460_1467delinsAGGTGGAC	XP_005254242.1:p.Lys487=
NM_000499.5:c.1460_1467delinsAGGTGGAC	NP_000490.1:p.Lys487=
NM_001319216.2:c.1373_1380delinsAGGTGGAC	NP_001306145.1:p.Lys458=
NM_001319217.2:c.1460_1467delinsAGGTGGAC MANE Select	NP_001306146.1:p.Lys487=