Canonical Allele Identifier: CA1729176774

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760920G= , CM000669.2:g.99760920G=	GRCh38
NC_000007.13:g.99358543G= , CM000669.1:g.99358543G=	GRCh37
NC_000007.12:g.99196479G=	NCBI36
NG_008421.1:g.28266C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1408C=	ENSP00000337915.3:p.Pro470=
ENST00000651162.1:n.750C=
ENST00000651514.1:c.1315C= MANE Select	ENSP00000498939.1:p.Pro439=
ENST00000651783.1:c.856C=	ENSP00000498924.1:p.Pro286=
ENST00000652018.1:c.1168C=	ENSP00000498733.1:p.Pro390=
ENST00000336411.6:c.1315C=	ENSP00000337915.2:p.Pro439=
ENST00000354593.6:c.865C=	ENSP00000346607.2:p.Pro289=
NM_001202855.2:c.1312C=	NP_001189784.1:p.Pro438=
NM_017460.5:c.1315C=	NP_059488.2:p.Pro439=
XM_011515841.1:c.1408C=	XP_011514143.1:p.Pro470=
XM_011515842.1:c.1405C=	XP_011514144.1:p.Pro469=
NM_017460.6:c.1315C= MANE Select	NP_059488.2:p.Pro439=
NM_001202855.3:c.1312C=	NP_001189784.1:p.Pro438=