Canonical Allele Identifier: CA1729176752

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760872C= , CM000669.2:g.99760872C=	GRCh38
NC_000007.13:g.99358495C= , CM000669.1:g.99358495C=	GRCh37
NC_000007.12:g.99196431C=	NCBI36
NG_008421.1:g.28314G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1456G=	ENSP00000337915.3:p.Ala486=
ENST00000651162.1:n.798G=
ENST00000651514.1:c.1363G= MANE Select	ENSP00000498939.1:p.Ala455=
ENST00000651783.1:c.904G=	ENSP00000498924.1:p.Ala302=
ENST00000652018.1:c.1216G=	ENSP00000498733.1:p.Ala406=
ENST00000336411.6:c.1363G=	ENSP00000337915.2:p.Ala455=
ENST00000354593.6:c.913G=	ENSP00000346607.2:p.Ala305=
NM_001202855.2:c.1360G=	NP_001189784.1:p.Ala454=
NM_017460.5:c.1363G=	NP_059488.2:p.Ala455=
XM_011515841.1:c.1456G=	XP_011514143.1:p.Ala486=
XM_011515842.1:c.1453G=	XP_011514144.1:p.Ala485=
NM_017460.6:c.1363G= MANE Select	NP_059488.2:p.Ala455=
NM_001202855.3:c.1360G=	NP_001189784.1:p.Ala454=