Canonical Allele Identifier: CA1729176763

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760890G= , CM000669.2:g.99760890G=	GRCh38
NC_000007.13:g.99358513G= , CM000669.1:g.99358513G=	GRCh37
NC_000007.12:g.99196449G=	NCBI36
NG_008421.1:g.28296C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1438C=	ENSP00000337915.3:p.Leu480=
ENST00000651162.1:n.780C=
ENST00000651514.1:c.1345C= MANE Select	ENSP00000498939.1:p.Leu449=
ENST00000651783.1:c.886C=	ENSP00000498924.1:p.Leu296=
ENST00000652018.1:c.1198C=	ENSP00000498733.1:p.Leu400=
ENST00000336411.6:c.1345C=	ENSP00000337915.2:p.Leu449=
ENST00000354593.6:c.895C=	ENSP00000346607.2:p.Leu299=
NM_001202855.2:c.1342C=	NP_001189784.1:p.Leu448=
NM_017460.5:c.1345C=	NP_059488.2:p.Leu449=
XM_011515841.1:c.1438C=	XP_011514143.1:p.Leu480=
XM_011515842.1:c.1435C=	XP_011514144.1:p.Leu479=
NM_017460.6:c.1345C= MANE Select	NP_059488.2:p.Leu449=
NM_001202855.3:c.1342C=	NP_001189784.1:p.Leu448=