Canonical Allele Identifier: CA1729179963

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767157C= , CM000669.2:g.99767157C=	GRCh38
NC_000007.13:g.99364780C= , CM000669.1:g.99364780C=	GRCh37
NC_000007.12:g.99202716C=	NCBI36
NG_008421.1:g.22029G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.772G=	ENSP00000337915.3:p.Glu258=
ENST00000651162.1:n.207G=
ENST00000651514.1:c.772G= MANE Select	ENSP00000498939.1:p.Glu258=
ENST00000651783.1:c.313G=	ENSP00000498924.1:p.Glu105=
ENST00000652018.1:c.625G=	ENSP00000498733.1:p.Glu209=
ENST00000336411.6:c.772G=	ENSP00000337915.2:p.Glu258=
ENST00000354593.6:c.322G=	ENSP00000346607.2:p.Glu108=
NM_001202855.2:c.769G=	NP_001189784.1:p.Glu257=
NM_017460.5:c.772G=	NP_059488.2:p.Glu258=
XM_011515841.1:c.772G=	XP_011514143.1:p.Glu258=
XM_011515842.1:c.769G=	XP_011514144.1:p.Glu257=
NM_017460.6:c.772G= MANE Select	NP_059488.2:p.Glu258=
NM_001202855.3:c.769G=	NP_001189784.1:p.Glu257=