Canonical Allele Identifier: CA1729176770

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760902T= , CM000669.2:g.99760902T=	GRCh38
NC_000007.13:g.99358525T= , CM000669.1:g.99358525T=	GRCh37
NC_000007.12:g.99196461T=	NCBI36
NG_008421.1:g.28284A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1426A=	ENSP00000337915.3:p.Met476=
ENST00000651162.1:n.768A=
ENST00000651514.1:c.1333A= MANE Select	ENSP00000498939.1:p.Met445=
ENST00000651783.1:c.874A=	ENSP00000498924.1:p.Met292=
ENST00000652018.1:c.1186A=	ENSP00000498733.1:p.Met396=
ENST00000336411.6:c.1333A=	ENSP00000337915.2:p.Met445=
ENST00000354593.6:c.883A=	ENSP00000346607.2:p.Met295=
NM_001202855.2:c.1330A=	NP_001189784.1:p.Met444=
NM_017460.5:c.1333A=	NP_059488.2:p.Met445=
XM_011515841.1:c.1426A=	XP_011514143.1:p.Met476=
XM_011515842.1:c.1423A=	XP_011514144.1:p.Met475=
NM_017460.6:c.1333A= MANE Select	NP_059488.2:p.Met445=
NM_001202855.3:c.1330A=	NP_001189784.1:p.Met444=