Canonical Allele Identifier: CA2187814885

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720557T= , CM000677.2:g.74720557T=	GRCh38
NC_000015.9:g.75012898T= , CM000677.1:g.75012898T=	GRCh37
NC_000015.8:g.72799951T=	NCBI36
NG_008431.1:g.3016T=
NG_008431.2:g.3016T=
NG_061374.1:g.9972A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1471A= MANE Select	ENSP00000369050.3:p.Thr491=
ENST00000379727.7:c.1471A=	ENSP00000369050.3:p.Thr491=
ENST00000395048.6:c.1471A=	ENSP00000378488.2:p.Thr491=
ENST00000395049.8:c.1384A=	ENSP00000378489.4:p.Thr462=
ENST00000567032.5:c.1471A=	ENSP00000456585.1:p.Thr491=
ENST00000612821.4:c.1387A=	ENSP00000479744.1:p.Thr463=
ENST00000617691.4:c.1384A=	ENSP00000482863.1:p.Thr462=
NM_000499.3:c.1471A=	NP_000490.1:p.Thr491=
XM_005254185.1:c.1471A=	XP_005254242.1:p.Thr491=
NM_000499.5:c.1471A=	NP_000490.1:p.Thr491=
NM_001319216.2:c.1384A=	NP_001306145.1:p.Thr462=
NM_001319217.2:c.1471A= MANE Select	NP_001306146.1:p.Thr491=