Canonical Allele Identifier: CA1729184591

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99772622T= , CM000669.2:g.99772622T=	GRCh38
NC_000007.13:g.99370245T= , CM000669.1:g.99370245T=	GRCh37
NC_000007.12:g.99208181T=	NCBI36
NG_008421.1:g.16564A=

Transcript Alleles

HGVS	Amino-acid Change
NM_017460.6:c.286A= MANE Select	NP_059488.2:p.Lys96=
ENST00000651514.1:c.286A= MANE Select	ENSP00000498939.1:p.Lys96=
NM_001202855.2:c.286A=	NP_001189784.1:p.Lys96=
NM_001202855.3:c.286A=	NP_001189784.1:p.Lys96=
NM_017460.5:c.286A=	NP_059488.2:p.Lys96=
ENST00000336411.6:c.286A=	ENSP00000337915.2:p.Lys96=
ENST00000336411.7:c.286A=	ENSP00000337915.3:p.Lys96=
ENST00000354593.6:c.72-4120A=	ENSP00000346607.2:n.72-4120A=
ENST00000415003.1:c.325A=	ENSP00000397208.1:p.Lys109=
ENST00000480043.1:n.183A=
ENST00000651783.1:c.58-4115A=	ENSP00000498924.1:n.58-4115A=
ENST00000652018.1:c.139A=	ENSP00000498733.1:p.Lys47=
XM_011515841.1:c.286A=	XP_011514143.1:p.Lys96=
XM_011515842.1:c.286A=	XP_011514144.1:p.Lys96=