Canonical Allele Identifier: CA368367516

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358446G>A (hg19) ; chr7:g.99760823G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760823G>A , CM000669.2:g.99760823G>A	GRCh38
NC_000007.13:g.99358446G>A , CM000669.1:g.99358446G>A	GRCh37
NC_000007.12:g.99196382G>A	NCBI36
NG_008421.1:g.28363C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1505C>T	ENSP00000337915.3:p.Thr502Ile
ENST00000651162.1:n.847C>T
ENST00000651514.1:c.1412C>T MANE Select	ENSP00000498939.1:p.Thr471Ile
ENST00000651783.1:c.953C>T	ENSP00000498924.1:p.Thr318Ile
ENST00000652018.1:c.1265C>T	ENSP00000498733.1:p.Thr422Ile
ENST00000336411.6:c.1412C>T	ENSP00000337915.2:p.Thr471Ile
ENST00000354593.6:c.962C>T	ENSP00000346607.2:p.Thr321Ile
NM_001202855.2:c.1409C>T	NP_001189784.1:p.Thr470Ile
NM_017460.5:c.1412C>T	NP_059488.2:p.Thr471Ile
XM_011515841.1:c.1505C>T	XP_011514143.1:p.Thr502Ile
XM_011515842.1:c.1502C>T	XP_011514144.1:p.Thr501Ile
NM_017460.6:c.1412C>T MANE Select	NP_059488.2:p.Thr471Ile
NM_001202855.3:c.1409C>T	NP_001189784.1:p.Thr470Ile