Canonical Allele Identifier: CA1729176784

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760940T= , CM000669.2:g.99760940T=	GRCh38
NC_000007.13:g.99358563T= , CM000669.1:g.99358563T=	GRCh37
NC_000007.12:g.99196499T=	NCBI36
NG_008421.1:g.28246A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1388A=	ENSP00000337915.3:p.Tyr463=
ENST00000651162.1:n.730A=
ENST00000651514.1:c.1295A= MANE Select	ENSP00000498939.1:p.Tyr432=
ENST00000651783.1:c.836A=	ENSP00000498924.1:p.Tyr279=
ENST00000652018.1:c.1148A=	ENSP00000498733.1:p.Tyr383=
ENST00000336411.6:c.1295A=	ENSP00000337915.2:p.Tyr432=
ENST00000354593.6:c.845A=	ENSP00000346607.2:p.Tyr282=
NM_001202855.2:c.1292A=	NP_001189784.1:p.Tyr431=
NM_017460.5:c.1295A=	NP_059488.2:p.Tyr432=
XM_011515841.1:c.1388A=	XP_011514143.1:p.Tyr463=
XM_011515842.1:c.1385A=	XP_011514144.1:p.Tyr462=
NM_017460.6:c.1295A= MANE Select	NP_059488.2:p.Tyr432=
NM_001202855.3:c.1292A=	NP_001189784.1:p.Tyr431=