Canonical Allele Identifier: CA1729179941

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767146G= , CM000669.2:g.99767146G=	GRCh38
NC_000007.13:g.99364769G= , CM000669.1:g.99364769G=	GRCh37
NC_000007.12:g.99202705G=	NCBI36
NG_008421.1:g.22040C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.783C=	ENSP00000337915.3:p.Leu261=
ENST00000651162.1:n.218C=
ENST00000651514.1:c.783C= MANE Select	ENSP00000498939.1:p.Leu261=
ENST00000651783.1:c.324C=	ENSP00000498924.1:p.Leu108=
ENST00000652018.1:c.636C=	ENSP00000498733.1:p.Leu212=
ENST00000336411.6:c.783C=	ENSP00000337915.2:p.Leu261=
ENST00000354593.6:c.333C=	ENSP00000346607.2:p.Leu111=
NM_001202855.2:c.780C=	NP_001189784.1:p.Leu260=
NM_017460.5:c.783C=	NP_059488.2:p.Leu261=
XM_011515841.1:c.783C=	XP_011514143.1:p.Leu261=
XM_011515842.1:c.780C=	XP_011514144.1:p.Leu260=
NM_017460.6:c.783C= MANE Select	NP_059488.2:p.Leu261=
NM_001202855.3:c.780C=	NP_001189784.1:p.Leu260=