Canonical Allele Identifier: CA456690217

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99367420T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769797T>A , CM000669.2:g.99769797T>A	GRCh38
NC_000007.13:g.99367420T>A , CM000669.1:g.99367420T>A	GRCh37
NC_000007.12:g.99205356T>A	NCBI36
NG_008421.1:g.19389A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.492A>T	ENSP00000337915.3:p.Ala164=
ENST00000651514.1:c.492A>T MANE Select	ENSP00000498939.1:p.Ala164=
ENST00000651783.1:c.58-1290A>T	ENSP00000498924.1:n.58-1290A>T
ENST00000652018.1:c.345A>T	ENSP00000498733.1:p.Ala115=
ENST00000336411.6:c.492A>T	ENSP00000337915.2:p.Ala164=
ENST00000354593.6:c.72-1295A>T	ENSP00000346607.2:n.72-1295A>T
ENST00000480043.1:n.389A>T
NM_001202855.2:c.492A>T	NP_001189784.1:p.Ala164=
NM_017460.5:c.492A>T	NP_059488.2:p.Ala164=
XM_011515841.1:c.492A>T	XP_011514143.1:p.Ala164=
XM_011515842.1:c.492A>T	XP_011514144.1:p.Ala164=
NM_017460.6:c.492A>T MANE Select	NP_059488.2:p.Ala164=
NM_001202855.3:c.492A>T	NP_001189784.1:p.Ala164=