Canonical Allele Identifier: CA1729176733

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760827C= , CM000669.2:g.99760827C=	GRCh38
NC_000007.13:g.99358450C= , CM000669.1:g.99358450C=	GRCh37
NC_000007.12:g.99196386C=	NCBI36
NG_008421.1:g.28359G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1501G=	ENSP00000337915.3:p.Glu501=
ENST00000651162.1:n.843G=
ENST00000651514.1:c.1408G= MANE Select	ENSP00000498939.1:p.Glu470=
ENST00000651783.1:c.949G=	ENSP00000498924.1:p.Glu317=
ENST00000652018.1:c.1261G=	ENSP00000498733.1:p.Glu421=
ENST00000336411.6:c.1408G=	ENSP00000337915.2:p.Glu470=
ENST00000354593.6:c.958G=	ENSP00000346607.2:p.Glu320=
NM_001202855.2:c.1405G=	NP_001189784.1:p.Glu469=
NM_017460.5:c.1408G=	NP_059488.2:p.Glu470=
XM_011515841.1:c.1501G=	XP_011514143.1:p.Glu501=
XM_011515842.1:c.1498G=	XP_011514144.1:p.Glu500=
NM_017460.6:c.1408G= MANE Select	NP_059488.2:p.Glu470=
NM_001202855.3:c.1405G=	NP_001189784.1:p.Glu469=