Canonical Allele Identifier: CA1729182585

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770202T= , CM000669.2:g.99770202T=	GRCh38
NC_000007.13:g.99367825T= , CM000669.1:g.99367825T=	GRCh37
NC_000007.12:g.99205761T=	NCBI36
NG_008421.1:g.18984A=

Transcript Alleles

HGVS	Amino-acid Change
NM_017460.6:c.352A= MANE Select	NP_059488.2:p.Ile118=
ENST00000651514.1:c.352A= MANE Select	ENSP00000498939.1:p.Ile118=
NM_001202855.2:c.352A=	NP_001189784.1:p.Ile118=
NM_001202855.3:c.352A=	NP_001189784.1:p.Ile118=
NM_017460.5:c.352A=	NP_059488.2:p.Ile118=
ENST00000336411.6:c.352A=	ENSP00000337915.2:p.Ile118=
ENST00000336411.7:c.352A=	ENSP00000337915.3:p.Ile118=
ENST00000354593.6:c.72-1700A=	ENSP00000346607.2:n.72-1700A=
ENST00000415003.1:c.391A=	ENSP00000397208.1:p.Ile131=
ENST00000480043.1:n.249A=
ENST00000651783.1:c.58-1695A=	ENSP00000498924.1:n.58-1695A=
ENST00000652018.1:c.205A=	ENSP00000498733.1:p.Ile69=
XM_011515841.1:c.352A=	XP_011514143.1:p.Ile118=
XM_011515842.1:c.352A=	XP_011514144.1:p.Ile118=