Canonical Allele Identifier: CA1729177271

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762020C= , CM000669.2:g.99762020C=	GRCh38
NC_000007.13:g.99359643C= , CM000669.1:g.99359643C=	GRCh37
NC_000007.12:g.99197579C=	NCBI36
NG_008421.1:g.27166G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1253+21G=	ENSP00000337915.3:n.1253+21G=
ENST00000651162.1:n.688+21G=
ENST00000651514.1:c.1253+21G= MANE Select	ENSP00000498939.1:n.1253+21G=
ENST00000651783.1:c.794+21G=	ENSP00000498924.1:n.794+21G=
ENST00000652018.1:c.1106+21G=	ENSP00000498733.1:n.1106+21G=
ENST00000336411.6:c.1253+21G=	ENSP00000337915.2:n.1253+21G=
ENST00000354593.6:c.803+21G=	ENSP00000346607.2:n.803+21G=
NM_001202855.2:c.1250+21G=	NP_001189784.1:n.1250+21G=
NM_017460.5:c.1253+21G=	NP_059488.2:n.1253+21G=
XM_011515841.1:c.1253+21G=	XP_011514143.1:n.1253+21G=
XM_011515842.1:c.1250+21G=	XP_011514144.1:n.1250+21G=
NM_017460.6:c.1253+21G= MANE Select	NP_059488.2:n.1253+21G=
NM_001202855.3:c.1250+21G=	NP_001189784.1:n.1250+21G=