Canonical Allele Identifier: CA1729180960

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768459A= , CM000669.2:g.99768459A=	GRCh38
NC_000007.13:g.99366082A= , CM000669.1:g.99366082A=	GRCh37
NC_000007.12:g.99204018A=	NCBI36
NG_008421.1:g.20727T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.565T=	ENSP00000337915.3:p.Phe189=
ENST00000651514.1:c.565T= MANE Select	ENSP00000498939.1:p.Phe189=
ENST00000651783.1:c.106T=	ENSP00000498924.1:p.Phe36=
ENST00000652018.1:c.418T=	ENSP00000498733.1:p.Phe140=
ENST00000336411.6:c.565T=	ENSP00000337915.2:p.Phe189=
ENST00000354593.6:c.115T=	ENSP00000346607.2:p.Phe39=
NM_001202855.2:c.565T=	NP_001189784.1:p.Phe189=
NM_017460.5:c.565T=	NP_059488.2:p.Phe189=
XM_011515841.1:c.565T=	XP_011514143.1:p.Phe189=
XM_011515842.1:c.565T=	XP_011514144.1:p.Phe189=
NM_017460.6:c.565T= MANE Select	NP_059488.2:p.Phe189=
NM_001202855.3:c.565T=	NP_001189784.1:p.Phe189=