Canonical Allele Identifier: CA1729176748

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760862C= , CM000669.2:g.99760862C=	GRCh38
NC_000007.13:g.99358485C= , CM000669.1:g.99358485C=	GRCh37
NC_000007.12:g.99196421C=	NCBI36
NG_008421.1:g.28324G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1466G=	ENSP00000337915.3:p.Arg489=
ENST00000651162.1:n.808G=
ENST00000651514.1:c.1373G= MANE Select	ENSP00000498939.1:p.Arg458=
ENST00000651783.1:c.914G=	ENSP00000498924.1:p.Arg305=
ENST00000652018.1:c.1226G=	ENSP00000498733.1:p.Arg409=
ENST00000336411.6:c.1373G=	ENSP00000337915.2:p.Arg458=
ENST00000354593.6:c.923G=	ENSP00000346607.2:p.Arg308=
NM_001202855.2:c.1370G=	NP_001189784.1:p.Arg457=
NM_017460.5:c.1373G=	NP_059488.2:p.Arg458=
XM_011515841.1:c.1466G=	XP_011514143.1:p.Arg489=
XM_011515842.1:c.1463G=	XP_011514144.1:p.Arg488=
NM_017460.6:c.1373G= MANE Select	NP_059488.2:p.Arg458=
NM_001202855.3:c.1370G=	NP_001189784.1:p.Arg457=