Canonical Allele Identifier: CA1729176807

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760986T= , CM000669.2:g.99760986T=	GRCh38
NC_000007.13:g.99358609T= , CM000669.1:g.99358609T=	GRCh37
NC_000007.12:g.99196545T=	NCBI36
NG_008421.1:g.28200A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1347-5A=	ENSP00000337915.3:n.1347-5A=
ENST00000651162.1:n.689-5A=
ENST00000651514.1:c.1254-5A= MANE Select	ENSP00000498939.1:n.1254-5A=
ENST00000651783.1:c.795-5A=	ENSP00000498924.1:n.795-5A=
ENST00000652018.1:c.1107-5A=	ENSP00000498733.1:n.1107-5A=
ENST00000336411.6:c.1254-5A=	ENSP00000337915.2:n.1254-5A=
ENST00000354593.6:c.804-5A=	ENSP00000346607.2:n.804-5A=
NM_001202855.2:c.1251-5A=	NP_001189784.1:n.1251-5A=
NM_017460.5:c.1254-5A=	NP_059488.2:n.1254-5A=
XM_011515841.1:c.1347-5A=	XP_011514143.1:n.1347-5A=
XM_011515842.1:c.1344-5A=	XP_011514144.1:n.1344-5A=
NM_017460.6:c.1254-5A= MANE Select	NP_059488.2:n.1254-5A=
NM_001202855.3:c.1251-5A=	NP_001189784.1:n.1251-5A=