Canonical Allele Identifier: CA1729176745

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760857G= , CM000669.2:g.99760857G=	GRCh38
NC_000007.13:g.99358480G= , CM000669.1:g.99358480G=	GRCh37
NC_000007.12:g.99196416G=	NCBI36
NG_008421.1:g.28329C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1471C=	ENSP00000337915.3:p.Leu491=
ENST00000651162.1:n.813C=
ENST00000651514.1:c.1378C= MANE Select	ENSP00000498939.1:p.Leu460=
ENST00000651783.1:c.919C=	ENSP00000498924.1:p.Leu307=
ENST00000652018.1:c.1231C=	ENSP00000498733.1:p.Leu411=
ENST00000336411.6:c.1378C=	ENSP00000337915.2:p.Leu460=
ENST00000354593.6:c.928C=	ENSP00000346607.2:p.Leu310=
NM_001202855.2:c.1375C=	NP_001189784.1:p.Leu459=
NM_017460.5:c.1378C=	NP_059488.2:p.Leu460=
XM_011515841.1:c.1471C=	XP_011514143.1:p.Leu491=
XM_011515842.1:c.1468C=	XP_011514144.1:p.Leu490=
NM_017460.6:c.1378C= MANE Select	NP_059488.2:p.Leu460=
NM_001202855.3:c.1375C=	NP_001189784.1:p.Leu459=