Canonical Allele Identifier: CA1729176742

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760845A= , CM000669.2:g.99760845A=	GRCh38
NC_000007.13:g.99358468A= , CM000669.1:g.99358468A=	GRCh37
NC_000007.12:g.99196404A=	NCBI36
NG_008421.1:g.28341T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1483T=	ENSP00000337915.3:p.Ser495=
ENST00000651162.1:n.825T=
ENST00000651514.1:c.1390T= MANE Select	ENSP00000498939.1:p.Ser464=
ENST00000651783.1:c.931T=	ENSP00000498924.1:p.Ser311=
ENST00000652018.1:c.1243T=	ENSP00000498733.1:p.Ser415=
ENST00000336411.6:c.1390T=	ENSP00000337915.2:p.Ser464=
ENST00000354593.6:c.940T=	ENSP00000346607.2:p.Ser314=
NM_001202855.2:c.1387T=	NP_001189784.1:p.Ser463=
NM_017460.5:c.1390T=	NP_059488.2:p.Ser464=
XM_011515841.1:c.1483T=	XP_011514143.1:p.Ser495=
XM_011515842.1:c.1480T=	XP_011514144.1:p.Ser494=
NM_017460.6:c.1390T= MANE Select	NP_059488.2:p.Ser464=
NM_001202855.3:c.1387T=	NP_001189784.1:p.Ser463=