Canonical Allele Identifier: CA2187814935

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720642_74720646delinsAATGG , CM000677.2:g.74720642_74720646delinsAATGG	GRCh38
NC_000015.9:g.75012983_75012987delinsAATGG , CM000677.1:g.75012983_75012987delinsAATGG	GRCh37
NC_000015.8:g.72800036_72800040delinsAATGG	NCBI36
NG_008431.1:g.3101_3105delinsAATGG
NG_008431.2:g.3101_3105delinsAATGG
NG_061374.1:g.9883_9887delinsCCATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000379727.8:c.1382_1386delinsCCATT MANE Select	ENSP00000369050.3:p.Thr461=
ENST00000379727.7:c.1382_1386delinsCCATT	ENSP00000369050.3:p.Thr461=
ENST00000395048.6:c.1382_1386delinsCCATT	ENSP00000378488.2:p.Thr461=
ENST00000395049.8:c.1295_1299delinsCCATT	ENSP00000378489.4:p.Thr432=
ENST00000567032.5:c.1382_1386delinsCCATT	ENSP00000456585.1:p.Thr461=
ENST00000612821.4:c.1298_1302delinsCCATT	ENSP00000479744.1:p.Thr433=
ENST00000617691.4:c.1295_1299delinsCCATT	ENSP00000482863.1:p.Thr432=
NM_000499.3:c.1382_1386delinsCCATT	NP_000490.1:p.Thr461=
XM_005254185.1:c.1382_1386delinsCCATT	XP_005254242.1:p.Thr461=
NM_000499.5:c.1382_1386delinsCCATT	NP_000490.1:p.Thr461=
NM_001319216.2:c.1295_1299delinsCCATT	NP_001306145.1:p.Thr432=
NM_001319217.2:c.1382_1386delinsCCATT MANE Select	NP_001306146.1:p.Thr461=