Canonical Allele Identifier: CA1729179975

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767165C= , CM000669.2:g.99767165C=	GRCh38
NC_000007.13:g.99364788C= , CM000669.1:g.99364788C=	GRCh37
NC_000007.12:g.99202724C=	NCBI36
NG_008421.1:g.22021G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.764G=	ENSP00000337915.3:p.Arg255=
ENST00000651162.1:n.199G=
ENST00000651514.1:c.764G= MANE Select	ENSP00000498939.1:p.Arg255=
ENST00000651783.1:c.305G=	ENSP00000498924.1:p.Arg102=
ENST00000652018.1:c.617G=	ENSP00000498733.1:p.Arg206=
ENST00000336411.6:c.764G=	ENSP00000337915.2:p.Arg255=
ENST00000354593.6:c.314G=	ENSP00000346607.2:p.Arg105=
NM_001202855.2:c.761G=	NP_001189784.1:p.Arg254=
NM_017460.5:c.764G=	NP_059488.2:p.Arg255=
XM_011515841.1:c.764G=	XP_011514143.1:p.Arg255=
XM_011515842.1:c.761G=	XP_011514144.1:p.Arg254=
NM_017460.6:c.764G= MANE Select	NP_059488.2:p.Arg255=
NM_001202855.3:c.761G=	NP_001189784.1:p.Arg254=