Canonical Allele Identifier: CA1729176753

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760874A= , CM000669.2:g.99760874A=	GRCh38
NC_000007.13:g.99358497A= , CM000669.1:g.99358497A=	GRCh37
NC_000007.12:g.99196433A=	NCBI36
NG_008421.1:g.28312T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1454T=	ENSP00000337915.3:p.Leu485=
ENST00000651162.1:n.796T=
ENST00000651514.1:c.1361T= MANE Select	ENSP00000498939.1:p.Leu454=
ENST00000651783.1:c.902T=	ENSP00000498924.1:p.Leu301=
ENST00000652018.1:c.1214T=	ENSP00000498733.1:p.Leu405=
ENST00000336411.6:c.1361T=	ENSP00000337915.2:p.Leu454=
ENST00000354593.6:c.911T=	ENSP00000346607.2:p.Leu304=
NM_001202855.2:c.1358T=	NP_001189784.1:p.Leu453=
NM_017460.5:c.1361T=	NP_059488.2:p.Leu454=
XM_011515841.1:c.1454T=	XP_011514143.1:p.Leu485=
XM_011515842.1:c.1451T=	XP_011514144.1:p.Leu484=
NM_017460.6:c.1361T= MANE Select	NP_059488.2:p.Leu454=
NM_001202855.3:c.1358T=	NP_001189784.1:p.Leu453=