Canonical Allele Identifier: CA1729176744

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760849G= , CM000669.2:g.99760849G=	GRCh38
NC_000007.13:g.99358472G= , CM000669.1:g.99358472G=	GRCh37
NC_000007.12:g.99196408G=	NCBI36
NG_008421.1:g.28337C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1479C=	ENSP00000337915.3:p.Asn493=
ENST00000651162.1:n.821C=
ENST00000651514.1:c.1386C= MANE Select	ENSP00000498939.1:p.Asn462=
ENST00000651783.1:c.927C=	ENSP00000498924.1:p.Asn309=
ENST00000652018.1:c.1239C=	ENSP00000498733.1:p.Asn413=
ENST00000336411.6:c.1386C=	ENSP00000337915.2:p.Asn462=
ENST00000354593.6:c.936C=	ENSP00000346607.2:p.Asn312=
NM_001202855.2:c.1383C=	NP_001189784.1:p.Asn461=
NM_017460.5:c.1386C=	NP_059488.2:p.Asn462=
XM_011515841.1:c.1479C=	XP_011514143.1:p.Asn493=
XM_011515842.1:c.1476C=	XP_011514144.1:p.Asn492=
NM_017460.6:c.1386C= MANE Select	NP_059488.2:p.Asn462=
NM_001202855.3:c.1383C=	NP_001189784.1:p.Asn461=