Canonical Allele Identifier: CA368368647

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358546C>T (hg19) ; chr7:g.99760923C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760923C>T , CM000669.2:g.99760923C>T	GRCh38
NC_000007.13:g.99358546C>T , CM000669.1:g.99358546C>T	GRCh37
NC_000007.12:g.99196482C>T	NCBI36
NG_008421.1:g.28263G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1405G>A	ENSP00000337915.3:p.Gly469Arg
ENST00000651162.1:n.747G>A
ENST00000651514.1:c.1312G>A MANE Select	ENSP00000498939.1:p.Gly438Arg
ENST00000651783.1:c.853G>A	ENSP00000498924.1:p.Gly285Arg
ENST00000652018.1:c.1165G>A	ENSP00000498733.1:p.Gly389Arg
ENST00000336411.6:c.1312G>A	ENSP00000337915.2:p.Gly438Arg
ENST00000354593.6:c.862G>A	ENSP00000346607.2:p.Gly288Arg
NM_001202855.2:c.1309G>A	NP_001189784.1:p.Gly437Arg
NM_017460.5:c.1312G>A	NP_059488.2:p.Gly438Arg
XM_011515841.1:c.1405G>A	XP_011514143.1:p.Gly469Arg
XM_011515842.1:c.1402G>A	XP_011514144.1:p.Gly468Arg
NM_017460.6:c.1312G>A MANE Select	NP_059488.2:p.Gly438Arg
NM_001202855.3:c.1309G>A	NP_001189784.1:p.Gly437Arg