Canonical Allele Identifier: CA1729176641

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760592A= , CM000669.2:g.99760592A=	GRCh38
NC_000007.13:g.99358215A= , CM000669.1:g.99358215A=	GRCh37
NC_000007.12:g.99196151A=	NCBI36
NG_008421.1:g.28594T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1509+227T=	ENSP00000337915.3:n.1509+227T=
ENST00000651162.1:n.851+227T=
ENST00000651514.1:c.1416+227T= MANE Select	ENSP00000498939.1:n.1416+227T=
ENST00000651783.1:c.957+227T=	ENSP00000498924.1:n.957+227T=
ENST00000652018.1:c.1269+227T=	ENSP00000498733.1:n.1269+227T=
ENST00000336411.6:c.1416+227T=	ENSP00000337915.2:n.1416+227T=
ENST00000354593.6:c.966+227T=	ENSP00000346607.2:n.966+227T=
NM_001202855.2:c.1413+227T=	NP_001189784.1:n.1413+227T=
NM_017460.5:c.1416+227T=	NP_059488.2:n.1416+227T=
XM_011515841.1:c.1509+227T=	XP_011514143.1:n.1509+227T=
XM_011515842.1:c.1506+227T=	XP_011514144.1:n.1506+227T=
NM_017460.6:c.1416+227T= MANE Select	NP_059488.2:n.1416+227T=
NM_001202855.3:c.1413+227T=	NP_001189784.1:n.1413+227T=