Canonical Allele Identifier: CA456686459

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358481G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760858G>T , CM000669.2:g.99760858G>T	GRCh38
NC_000007.13:g.99358481G>T , CM000669.1:g.99358481G>T	GRCh37
NC_000007.12:g.99196417G>T	NCBI36
NG_008421.1:g.28328C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1470C>A	ENSP00000337915.3:p.Val490=
ENST00000651162.1:n.812C>A
ENST00000651514.1:c.1377C>A MANE Select	ENSP00000498939.1:p.Val459=
ENST00000651783.1:c.918C>A	ENSP00000498924.1:p.Val306=
ENST00000652018.1:c.1230C>A	ENSP00000498733.1:p.Val410=
ENST00000336411.6:c.1377C>A	ENSP00000337915.2:p.Val459=
ENST00000354593.6:c.927C>A	ENSP00000346607.2:p.Val309=
NM_001202855.2:c.1374C>A	NP_001189784.1:p.Val458=
NM_017460.5:c.1377C>A	NP_059488.2:p.Val459=
XM_011515841.1:c.1470C>A	XP_011514143.1:p.Val490=
XM_011515842.1:c.1467C>A	XP_011514144.1:p.Val489=
NM_017460.6:c.1377C>A MANE Select	NP_059488.2:p.Val459=
NM_001202855.3:c.1374C>A	NP_001189784.1:p.Val458=