Canonical Allele Identifier: CA1729176736

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760833A= , CM000669.2:g.99760833A=	GRCh38
NC_000007.13:g.99358456A= , CM000669.1:g.99358456A=	GRCh37
NC_000007.12:g.99196392A=	NCBI36
NG_008421.1:g.28353T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1495T=	ENSP00000337915.3:p.Cys499=
ENST00000651162.1:n.837T=
ENST00000651514.1:c.1402T= MANE Select	ENSP00000498939.1:p.Cys468=
ENST00000651783.1:c.943T=	ENSP00000498924.1:p.Cys315=
ENST00000652018.1:c.1255T=	ENSP00000498733.1:p.Cys419=
ENST00000336411.6:c.1402T=	ENSP00000337915.2:p.Cys468=
ENST00000354593.6:c.952T=	ENSP00000346607.2:p.Cys318=
NM_001202855.2:c.1399T=	NP_001189784.1:p.Cys467=
NM_017460.5:c.1402T=	NP_059488.2:p.Cys468=
XM_011515841.1:c.1495T=	XP_011514143.1:p.Cys499=
XM_011515842.1:c.1492T=	XP_011514144.1:p.Cys498=
NM_017460.6:c.1402T= MANE Select	NP_059488.2:p.Cys468=
NM_001202855.3:c.1399T=	NP_001189784.1:p.Cys467=