Canonical Allele Identifier: CA1729177345

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762189T= , CM000669.2:g.99762189T=	GRCh38
NC_000007.13:g.99359812T= , CM000669.1:g.99359812T=	GRCh37
NC_000007.12:g.99197748T=	NCBI36
NG_008421.1:g.26997A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1105A=	ENSP00000337915.3:p.Ile369=
ENST00000651162.1:n.540A=
ENST00000651514.1:c.1105A= MANE Select	ENSP00000498939.1:p.Ile369=
ENST00000651783.1:c.646A=	ENSP00000498924.1:p.Ile216=
ENST00000652018.1:c.958A=	ENSP00000498733.1:p.Ile320=
ENST00000336411.6:c.1105A=	ENSP00000337915.2:p.Ile369=
ENST00000354593.6:c.655A=	ENSP00000346607.2:p.Ile219=
NM_001202855.2:c.1102A=	NP_001189784.1:p.Ile368=
NM_017460.5:c.1105A=	NP_059488.2:p.Ile369=
XM_011515841.1:c.1105A=	XP_011514143.1:p.Ile369=
XM_011515842.1:c.1102A=	XP_011514144.1:p.Ile368=
NM_017460.6:c.1105A= MANE Select	NP_059488.2:p.Ile369=
NM_001202855.3:c.1102A=	NP_001189784.1:p.Ile368=