Canonical Allele Identifier: CA1729179947

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767151G= , CM000669.2:g.99767151G=	GRCh38
NC_000007.13:g.99364774G= , CM000669.1:g.99364774G=	GRCh37
NC_000007.12:g.99202710G=	NCBI36
NG_008421.1:g.22035C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.778C=	ENSP00000337915.3:p.Arg260=
ENST00000651162.1:n.213C=
ENST00000651514.1:c.778C= MANE Select	ENSP00000498939.1:p.Arg260=
ENST00000651783.1:c.319C=	ENSP00000498924.1:p.Arg107=
ENST00000652018.1:c.631C=	ENSP00000498733.1:p.Arg211=
ENST00000336411.6:c.778C=	ENSP00000337915.2:p.Arg260=
ENST00000354593.6:c.328C=	ENSP00000346607.2:p.Arg110=
NM_001202855.2:c.775C=	NP_001189784.1:p.Arg259=
NM_017460.5:c.778C=	NP_059488.2:p.Arg260=
XM_011515841.1:c.778C=	XP_011514143.1:p.Arg260=
XM_011515842.1:c.775C=	XP_011514144.1:p.Arg259=
NM_017460.6:c.778C= MANE Select	NP_059488.2:p.Arg260=
NM_001202855.3:c.775C=	NP_001189784.1:p.Arg259=