Canonical Allele Identifier: CA456686594

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358514A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760891A>T , CM000669.2:g.99760891A>T	GRCh38
NC_000007.13:g.99358514A>T , CM000669.1:g.99358514A>T	GRCh37
NC_000007.12:g.99196450A>T	NCBI36
NG_008421.1:g.28295T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1437T>A	ENSP00000337915.3:p.Ala479=
ENST00000651162.1:n.779T>A
ENST00000651514.1:c.1344T>A MANE Select	ENSP00000498939.1:p.Ala448=
ENST00000651783.1:c.885T>A	ENSP00000498924.1:p.Ala295=
ENST00000652018.1:c.1197T>A	ENSP00000498733.1:p.Ala399=
ENST00000336411.6:c.1344T>A	ENSP00000337915.2:p.Ala448=
ENST00000354593.6:c.894T>A	ENSP00000346607.2:p.Ala298=
NM_001202855.2:c.1341T>A	NP_001189784.1:p.Ala447=
NM_017460.5:c.1344T>A	NP_059488.2:p.Ala448=
XM_011515841.1:c.1437T>A	XP_011514143.1:p.Ala479=
XM_011515842.1:c.1434T>A	XP_011514144.1:p.Ala478=
NM_017460.6:c.1344T>A MANE Select	NP_059488.2:p.Ala448=
NM_001202855.3:c.1341T>A	NP_001189784.1:p.Ala447=