Canonical Allele Identifier: CA368368601

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358527C>A (hg19) ; chr7:g.99760904C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760904C>A , CM000669.2:g.99760904C>A	GRCh38
NC_000007.13:g.99358527C>A , CM000669.1:g.99358527C>A	GRCh37
NC_000007.12:g.99196463C>A	NCBI36
NG_008421.1:g.28282G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1424G>T	ENSP00000337915.3:p.Gly475Val
ENST00000651162.1:n.766G>T
ENST00000651514.1:c.1331G>T MANE Select	ENSP00000498939.1:p.Gly444Val
ENST00000651783.1:c.872G>T	ENSP00000498924.1:p.Gly291Val
ENST00000652018.1:c.1184G>T	ENSP00000498733.1:p.Gly395Val
ENST00000336411.6:c.1331G>T	ENSP00000337915.2:p.Gly444Val
ENST00000354593.6:c.881G>T	ENSP00000346607.2:p.Gly294Val
NM_001202855.2:c.1328G>T	NP_001189784.1:p.Gly443Val
NM_017460.5:c.1331G>T	NP_059488.2:p.Gly444Val
XM_011515841.1:c.1424G>T	XP_011514143.1:p.Gly475Val
XM_011515842.1:c.1421G>T	XP_011514144.1:p.Gly474Val
NM_017460.6:c.1331G>T MANE Select	NP_059488.2:p.Gly444Val
NM_001202855.3:c.1328G>T	NP_001189784.1:p.Gly443Val