Canonical Allele Identifier: CA1729182155

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769773C= , CM000669.2:g.99769773C=	GRCh38
NC_000007.13:g.99367396C= , CM000669.1:g.99367396C=	GRCh37
NC_000007.12:g.99205332C=	NCBI36
NG_008421.1:g.19413G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.516G=	ENSP00000337915.3:p.Leu172=
ENST00000651514.1:c.516G= MANE Select	ENSP00000498939.1:p.Leu172=
ENST00000651783.1:c.58-1266G=	ENSP00000498924.1:n.58-1266G=
ENST00000652018.1:c.369G=	ENSP00000498733.1:p.Leu123=
ENST00000336411.6:c.516G=	ENSP00000337915.2:p.Leu172=
ENST00000354593.6:c.72-1271G=	ENSP00000346607.2:n.72-1271G=
ENST00000480043.1:n.413G=
NM_001202855.2:c.516G=	NP_001189784.1:p.Leu172=
NM_017460.5:c.516G=	NP_059488.2:p.Leu172=
XM_011515841.1:c.516G=	XP_011514143.1:p.Leu172=
XM_011515842.1:c.516G=	XP_011514144.1:p.Leu172=
NM_017460.6:c.516G= MANE Select	NP_059488.2:p.Leu172=
NM_001202855.3:c.516G=	NP_001189784.1:p.Leu172=