Canonical Allele Identifier: CA1729180035

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767222A= , CM000669.2:g.99767222A=	GRCh38
NC_000007.13:g.99364845A= , CM000669.1:g.99364845A=	GRCh37
NC_000007.12:g.99202781A=	NCBI36
NG_008421.1:g.21964T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.707T=	ENSP00000337915.3:p.Leu236=
ENST00000651162.1:n.142T=
ENST00000651514.1:c.707T= MANE Select	ENSP00000498939.1:p.Leu236=
ENST00000651783.1:c.248T=	ENSP00000498924.1:p.Leu83=
ENST00000652018.1:c.560T=	ENSP00000498733.1:p.Leu187=
ENST00000336411.6:c.707T=	ENSP00000337915.2:p.Leu236=
ENST00000354593.6:c.257T=	ENSP00000346607.2:p.Leu86=
NM_001202855.2:c.704T=	NP_001189784.1:p.Leu235=
NM_017460.5:c.707T=	NP_059488.2:p.Leu236=
XM_011515841.1:c.707T=	XP_011514143.1:p.Leu236=
XM_011515842.1:c.704T=	XP_011514144.1:p.Leu235=
NM_017460.6:c.707T= MANE Select	NP_059488.2:p.Leu236=
NM_001202855.3:c.704T=	NP_001189784.1:p.Leu235=