Canonical Allele Identifier: CA1729180047

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767235T= , CM000669.2:g.99767235T=	GRCh38
NC_000007.13:g.99364858T= , CM000669.1:g.99364858T=	GRCh37
NC_000007.12:g.99202794T=	NCBI36
NG_008421.1:g.21951A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.694A=	ENSP00000337915.3:p.Ile232=
ENST00000651162.1:n.129A=
ENST00000651514.1:c.694A= MANE Select	ENSP00000498939.1:p.Ile232=
ENST00000651783.1:c.235A=	ENSP00000498924.1:p.Ile79=
ENST00000652018.1:c.547A=	ENSP00000498733.1:p.Ile183=
ENST00000336411.6:c.694A=	ENSP00000337915.2:p.Ile232=
ENST00000354593.6:c.244A=	ENSP00000346607.2:p.Ile82=
NM_001202855.2:c.691A=	NP_001189784.1:p.Ile231=
NM_017460.5:c.694A=	NP_059488.2:p.Ile232=
XM_011515841.1:c.694A=	XP_011514143.1:p.Ile232=
XM_011515842.1:c.691A=	XP_011514144.1:p.Ile231=
NM_017460.6:c.694A= MANE Select	NP_059488.2:p.Ile232=
NM_001202855.3:c.691A=	NP_001189784.1:p.Ile231=