Canonical Allele Identifier: CA1729176749

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760863T= , CM000669.2:g.99760863T=	GRCh38
NC_000007.13:g.99358486T= , CM000669.1:g.99358486T=	GRCh37
NC_000007.12:g.99196422T=	NCBI36
NG_008421.1:g.28323A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1465A=	ENSP00000337915.3:p.Arg489=
ENST00000651162.1:n.807A=
ENST00000651514.1:c.1372A= MANE Select	ENSP00000498939.1:p.Arg458=
ENST00000651783.1:c.913A=	ENSP00000498924.1:p.Arg305=
ENST00000652018.1:c.1225A=	ENSP00000498733.1:p.Arg409=
ENST00000336411.6:c.1372A=	ENSP00000337915.2:p.Arg458=
ENST00000354593.6:c.922A=	ENSP00000346607.2:p.Arg308=
NM_001202855.2:c.1369A=	NP_001189784.1:p.Arg457=
NM_017460.5:c.1372A=	NP_059488.2:p.Arg458=
XM_011515841.1:c.1465A=	XP_011514143.1:p.Arg489=
XM_011515842.1:c.1462A=	XP_011514144.1:p.Arg488=
NM_017460.6:c.1372A= MANE Select	NP_059488.2:p.Arg458=
NM_001202855.3:c.1369A=	NP_001189784.1:p.Arg457=