Canonical Allele Identifier: CA1729176778

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760929C= , CM000669.2:g.99760929C=	GRCh38
NC_000007.13:g.99358552C= , CM000669.1:g.99358552C=	GRCh37
NC_000007.12:g.99196488C=	NCBI36
NG_008421.1:g.28257G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1399G=	ENSP00000337915.3:p.Gly467=
ENST00000651162.1:n.741G=
ENST00000651514.1:c.1306G= MANE Select	ENSP00000498939.1:p.Gly436=
ENST00000651783.1:c.847G=	ENSP00000498924.1:p.Gly283=
ENST00000652018.1:c.1159G=	ENSP00000498733.1:p.Gly387=
ENST00000336411.6:c.1306G=	ENSP00000337915.2:p.Gly436=
ENST00000354593.6:c.856G=	ENSP00000346607.2:p.Gly286=
NM_001202855.2:c.1303G=	NP_001189784.1:p.Gly435=
NM_017460.5:c.1306G=	NP_059488.2:p.Gly436=
XM_011515841.1:c.1399G=	XP_011514143.1:p.Gly467=
XM_011515842.1:c.1396G=	XP_011514144.1:p.Gly466=
NM_017460.6:c.1306G= MANE Select	NP_059488.2:p.Gly436=
NM_001202855.3:c.1303G=	NP_001189784.1:p.Gly435=