Canonical Allele Identifier: CA1729179966

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767158T= , CM000669.2:g.99767158T=	GRCh38
NC_000007.13:g.99364781T= , CM000669.1:g.99364781T=	GRCh37
NC_000007.12:g.99202717T=	NCBI36
NG_008421.1:g.22028A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.771A=	ENSP00000337915.3:p.Lys257=
ENST00000651162.1:n.206A=
ENST00000651514.1:c.771A= MANE Select	ENSP00000498939.1:p.Lys257=
ENST00000651783.1:c.312A=	ENSP00000498924.1:p.Lys104=
ENST00000652018.1:c.624A=	ENSP00000498733.1:p.Lys208=
ENST00000336411.6:c.771A=	ENSP00000337915.2:p.Lys257=
ENST00000354593.6:c.321A=	ENSP00000346607.2:p.Lys107=
NM_001202855.2:c.768A=	NP_001189784.1:p.Lys256=
NM_017460.5:c.771A=	NP_059488.2:p.Lys257=
XM_011515841.1:c.771A=	XP_011514143.1:p.Lys257=
XM_011515842.1:c.768A=	XP_011514144.1:p.Lys256=
NM_017460.6:c.771A= MANE Select	NP_059488.2:p.Lys257=
NM_001202855.3:c.768A=	NP_001189784.1:p.Lys256=