Canonical Allele Identifier: CA1729182506

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770153G= , CM000669.2:g.99770153G=	GRCh38
NC_000007.13:g.99367776G= , CM000669.1:g.99367776G=	GRCh37
NC_000007.12:g.99205712G=	NCBI36
NG_008421.1:g.19033C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.401C=	ENSP00000337915.3:p.Ser134=
ENST00000651514.1:c.401C= MANE Select	ENSP00000498939.1:p.Ser134=
ENST00000651783.1:c.58-1646C=	ENSP00000498924.1:n.58-1646C=
ENST00000652018.1:c.254C=	ENSP00000498733.1:p.Ser85=
ENST00000336411.6:c.401C=	ENSP00000337915.2:p.Ser134=
ENST00000354593.6:c.72-1651C=	ENSP00000346607.2:n.72-1651C=
ENST00000415003.1:c.440C=	ENSP00000397208.1:p.Ser147=
ENST00000480043.1:n.298C=
NM_001202855.2:c.401C=	NP_001189784.1:p.Ser134=
NM_017460.5:c.401C=	NP_059488.2:p.Ser134=
XM_011515841.1:c.401C=	XP_011514143.1:p.Ser134=
XM_011515842.1:c.401C=	XP_011514144.1:p.Ser134=
NM_017460.6:c.401C= MANE Select	NP_059488.2:p.Ser134=
NM_001202855.3:c.401C=	NP_001189784.1:p.Ser134=