Canonical Allele Identifier: CA368368577

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358516C>T (hg19) ; chr7:g.99760893C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760893C>T , CM000669.2:g.99760893C>T	GRCh38
NC_000007.13:g.99358516C>T , CM000669.1:g.99358516C>T	GRCh37
NC_000007.12:g.99196452C>T	NCBI36
NG_008421.1:g.28293G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1435G>A	ENSP00000337915.3:p.Ala479Thr
ENST00000651162.1:n.777G>A
ENST00000651514.1:c.1342G>A MANE Select	ENSP00000498939.1:p.Ala448Thr
ENST00000651783.1:c.883G>A	ENSP00000498924.1:p.Ala295Thr
ENST00000652018.1:c.1195G>A	ENSP00000498733.1:p.Ala399Thr
ENST00000336411.6:c.1342G>A	ENSP00000337915.2:p.Ala448Thr
ENST00000354593.6:c.892G>A	ENSP00000346607.2:p.Ala298Thr
NM_001202855.2:c.1339G>A	NP_001189784.1:p.Ala447Thr
NM_017460.5:c.1342G>A	NP_059488.2:p.Ala448Thr
XM_011515841.1:c.1435G>A	XP_011514143.1:p.Ala479Thr
XM_011515842.1:c.1432G>A	XP_011514144.1:p.Ala478Thr
NM_017460.6:c.1342G>A MANE Select	NP_059488.2:p.Ala448Thr
NM_001202855.3:c.1339G>A	NP_001189784.1:p.Ala447Thr