Canonical Allele Identifier: CA1729176767

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760898C= , CM000669.2:g.99760898C=	GRCh38
NC_000007.13:g.99358521C= , CM000669.1:g.99358521C=	GRCh37
NC_000007.12:g.99196457C=	NCBI36
NG_008421.1:g.28288G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1430G=	ENSP00000337915.3:p.Arg477=
ENST00000651162.1:n.772G=
ENST00000651514.1:c.1337G= MANE Select	ENSP00000498939.1:p.Arg446=
ENST00000651783.1:c.878G=	ENSP00000498924.1:p.Arg293=
ENST00000652018.1:c.1190G=	ENSP00000498733.1:p.Arg397=
ENST00000336411.6:c.1337G=	ENSP00000337915.2:p.Arg446=
ENST00000354593.6:c.887G=	ENSP00000346607.2:p.Arg296=
NM_001202855.2:c.1334G=	NP_001189784.1:p.Arg445=
NM_017460.5:c.1337G=	NP_059488.2:p.Arg446=
XM_011515841.1:c.1430G=	XP_011514143.1:p.Arg477=
XM_011515842.1:c.1427G=	XP_011514144.1:p.Arg476=
NM_017460.6:c.1337G= MANE Select	NP_059488.2:p.Arg446=
NM_001202855.3:c.1334G=	NP_001189784.1:p.Arg445=