Canonical Allele Identifier: CA1729182338

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769983C= , CM000669.2:g.99769983C=	GRCh38
NC_000007.13:g.99367606C= , CM000669.1:g.99367606C=	GRCh37
NC_000007.12:g.99205542C=	NCBI36
NG_008421.1:g.19203G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.433-127G=	ENSP00000337915.3:n.433-127G=
ENST00000651514.1:c.433-127G= MANE Select	ENSP00000498939.1:n.433-127G=
ENST00000651783.1:c.58-1476G=	ENSP00000498924.1:n.58-1476G=
ENST00000652018.1:c.286-127G=	ENSP00000498733.1:n.286-127G=
ENST00000336411.6:c.433-127G=	ENSP00000337915.2:n.433-127G=
ENST00000354593.6:c.72-1481G=	ENSP00000346607.2:n.72-1481G=
ENST00000480043.1:n.330-127G=
NM_001202855.2:c.433-127G=	NP_001189784.1:n.433-127G=
NM_017460.5:c.433-127G=	NP_059488.2:n.433-127G=
XM_011515841.1:c.433-127G=	XP_011514143.1:n.433-127G=
XM_011515842.1:c.433-127G=	XP_011514144.1:n.433-127G=
NM_017460.6:c.433-127G= MANE Select	NP_059488.2:n.433-127G=
NM_001202855.3:c.433-127G=	NP_001189784.1:n.433-127G=