Canonical Allele Identifier: CA456686466

Gene: CYP3A4

Linked Data

• COSMIC: COSM453675
• MyVariant Identifiers: chr7:g.99358487G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760864G>T , CM000669.2:g.99760864G>T	GRCh38
NC_000007.13:g.99358487G>T , CM000669.1:g.99358487G>T	GRCh37
NC_000007.12:g.99196423G>T	NCBI36
NG_008421.1:g.28322C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1464C>A	ENSP00000337915.3:p.Ile488=
ENST00000651162.1:n.806C>A
ENST00000651514.1:c.1371C>A MANE Select	ENSP00000498939.1:p.Ile457=
ENST00000651783.1:c.912C>A	ENSP00000498924.1:p.Ile304=
ENST00000652018.1:c.1224C>A	ENSP00000498733.1:p.Ile408=
ENST00000336411.6:c.1371C>A	ENSP00000337915.2:p.Ile457=
ENST00000354593.6:c.921C>A	ENSP00000346607.2:p.Ile307=
NM_001202855.2:c.1368C>A	NP_001189784.1:p.Ile456=
NM_017460.5:c.1371C>A	NP_059488.2:p.Ile457=
XM_011515841.1:c.1464C>A	XP_011514143.1:p.Ile488=
XM_011515842.1:c.1461C>A	XP_011514144.1:p.Ile487=
NM_017460.6:c.1371C>A MANE Select	NP_059488.2:p.Ile457=
NM_001202855.3:c.1368C>A	NP_001189784.1:p.Ile456=