Canonical Allele Identifier: CA1729176795

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760962C= , CM000669.2:g.99760962C=	GRCh38
NC_000007.13:g.99358585C= , CM000669.1:g.99358585C=	GRCh37
NC_000007.12:g.99196521C=	NCBI36
NG_008421.1:g.28224G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1366G=	ENSP00000337915.3:p.Asp456=
ENST00000651162.1:n.708G=
ENST00000651514.1:c.1273G= MANE Select	ENSP00000498939.1:p.Asp425=
ENST00000651783.1:c.814G=	ENSP00000498924.1:p.Asp272=
ENST00000652018.1:c.1126G=	ENSP00000498733.1:p.Asp376=
ENST00000336411.6:c.1273G=	ENSP00000337915.2:p.Asp425=
ENST00000354593.6:c.823G=	ENSP00000346607.2:p.Asp275=
NM_001202855.2:c.1270G=	NP_001189784.1:p.Asp424=
NM_017460.5:c.1273G=	NP_059488.2:p.Asp425=
XM_011515841.1:c.1366G=	XP_011514143.1:p.Asp456=
XM_011515842.1:c.1363G=	XP_011514144.1:p.Asp455=
NM_017460.6:c.1273G= MANE Select	NP_059488.2:p.Asp425=
NM_001202855.3:c.1270G=	NP_001189784.1:p.Asp424=