Canonical Allele Identifier: CA1729176766

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760894A= , CM000669.2:g.99760894A=	GRCh38
NC_000007.13:g.99358517A= , CM000669.1:g.99358517A=	GRCh37
NC_000007.12:g.99196453A=	NCBI36
NG_008421.1:g.28292T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1434T=	ENSP00000337915.3:p.Phe478=
ENST00000651162.1:n.776T=
ENST00000651514.1:c.1341T= MANE Select	ENSP00000498939.1:p.Phe447=
ENST00000651783.1:c.882T=	ENSP00000498924.1:p.Phe294=
ENST00000652018.1:c.1194T=	ENSP00000498733.1:p.Phe398=
ENST00000336411.6:c.1341T=	ENSP00000337915.2:p.Phe447=
ENST00000354593.6:c.891T=	ENSP00000346607.2:p.Phe297=
NM_001202855.2:c.1338T=	NP_001189784.1:p.Phe446=
NM_017460.5:c.1341T=	NP_059488.2:p.Phe447=
XM_011515841.1:c.1434T=	XP_011514143.1:p.Phe478=
XM_011515842.1:c.1431T=	XP_011514144.1:p.Phe477=
NM_017460.6:c.1341T= MANE Select	NP_059488.2:p.Phe447=
NM_001202855.3:c.1338T=	NP_001189784.1:p.Phe446=