Canonical Allele Identifier: CA456686415

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358442C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760819C>T , CM000669.2:g.99760819C>T	GRCh38
NC_000007.13:g.99358442C>T , CM000669.1:g.99358442C>T	GRCh37
NC_000007.12:g.99196378C>T	NCBI36
NG_008421.1:g.28367G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1509G>A	ENSP00000337915.3:p.Gln503=
ENST00000651162.1:n.851G>A
ENST00000651514.1:c.1416G>A MANE Select	ENSP00000498939.1:p.Gln472=
ENST00000651783.1:c.957G>A	ENSP00000498924.1:p.Gln319=
ENST00000652018.1:c.1269G>A	ENSP00000498733.1:p.Gln423=
ENST00000336411.6:c.1416G>A	ENSP00000337915.2:p.Gln472=
ENST00000354593.6:c.966G>A	ENSP00000346607.2:p.Gln322=
NM_001202855.2:c.1413G>A	NP_001189784.1:p.Gln471=
NM_017460.5:c.1416G>A	NP_059488.2:p.Gln472=
XM_011515841.1:c.1509G>A	XP_011514143.1:p.Gln503=
XM_011515842.1:c.1506G>A	XP_011514144.1:p.Gln502=
NM_017460.6:c.1416G>A MANE Select	NP_059488.2:p.Gln472=
NM_001202855.3:c.1413G>A	NP_001189784.1:p.Gln471=