Canonical Allele Identifier: CA368368666

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358555A>C (hg19) ; chr7:g.99760932A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760932A>C , CM000669.2:g.99760932A>C	GRCh38
NC_000007.13:g.99358555A>C , CM000669.1:g.99358555A>C	GRCh37
NC_000007.12:g.99196491A>C	NCBI36
NG_008421.1:g.28254T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1396T>G	ENSP00000337915.3:p.Phe466Val
ENST00000651162.1:n.738T>G
ENST00000651514.1:c.1303T>G MANE Select	ENSP00000498939.1:p.Phe435Val
ENST00000651783.1:c.844T>G	ENSP00000498924.1:p.Phe282Val
ENST00000652018.1:c.1156T>G	ENSP00000498733.1:p.Phe386Val
ENST00000336411.6:c.1303T>G	ENSP00000337915.2:p.Phe435Val
ENST00000354593.6:c.853T>G	ENSP00000346607.2:p.Phe285Val
NM_001202855.2:c.1300T>G	NP_001189784.1:p.Phe434Val
NM_017460.5:c.1303T>G	NP_059488.2:p.Phe435Val
XM_011515841.1:c.1396T>G	XP_011514143.1:p.Phe466Val
XM_011515842.1:c.1393T>G	XP_011514144.1:p.Phe465Val
NM_017460.6:c.1303T>G MANE Select	NP_059488.2:p.Phe435Val
NM_001202855.3:c.1300T>G	NP_001189784.1:p.Phe434Val