Canonical Allele Identifier: CA1729182487

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770146G= , CM000669.2:g.99770146G=	GRCh38
NC_000007.13:g.99367769G= , CM000669.1:g.99367769G=	GRCh37
NC_000007.12:g.99205705G=	NCBI36
NG_008421.1:g.19040C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.408C=	ENSP00000337915.3:p.Thr136=
ENST00000651514.1:c.408C= MANE Select	ENSP00000498939.1:p.Thr136=
ENST00000651783.1:c.58-1639C=	ENSP00000498924.1:n.58-1639C=
ENST00000652018.1:c.261C=	ENSP00000498733.1:p.Thr87=
ENST00000336411.6:c.408C=	ENSP00000337915.2:p.Thr136=
ENST00000354593.6:c.72-1644C=	ENSP00000346607.2:n.72-1644C=
ENST00000415003.1:c.447C=	ENSP00000397208.1:p.Thr149=
ENST00000480043.1:n.305C=
NM_001202855.2:c.408C=	NP_001189784.1:p.Thr136=
NM_017460.5:c.408C=	NP_059488.2:p.Thr136=
XM_011515841.1:c.408C=	XP_011514143.1:p.Thr136=
XM_011515842.1:c.408C=	XP_011514144.1:p.Thr136=
NM_017460.6:c.408C= MANE Select	NP_059488.2:p.Thr136=
NM_001202855.3:c.408C=	NP_001189784.1:p.Thr136=