Canonical Allele Identifier: CA1729180204

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767449T= , CM000669.2:g.99767449T=	GRCh38
NC_000007.13:g.99365072T= , CM000669.1:g.99365072T=	GRCh37
NC_000007.12:g.99203008T=	NCBI36
NG_008421.1:g.21737A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.671-191A=	ENSP00000337915.3:n.671-191A=
ENST00000651162.1:n.106-191A=
ENST00000651514.1:c.671-191A= MANE Select	ENSP00000498939.1:n.671-191A=
ENST00000651783.1:c.212-191A=	ENSP00000498924.1:n.212-191A=
ENST00000652018.1:c.524-191A=	ENSP00000498733.1:n.524-191A=
ENST00000336411.6:c.671-191A=	ENSP00000337915.2:n.671-191A=
ENST00000354593.6:c.221-191A=	ENSP00000346607.2:n.221-191A=
NM_001202855.2:c.671-194A=	NP_001189784.1:n.671-194A=
NM_017460.5:c.671-191A=	NP_059488.2:n.671-191A=
XM_011515841.1:c.671-191A=	XP_011514143.1:n.671-191A=
XM_011515842.1:c.671-194A=	XP_011514144.1:n.671-194A=
NM_017460.6:c.671-191A= MANE Select	NP_059488.2:n.671-191A=
NM_001202855.3:c.671-194A=	NP_001189784.1:n.671-194A=