Canonical Allele Identifier: CA368368772

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358602A>C (hg19) ; chr7:g.99760979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760979A>C , CM000669.2:g.99760979A>C	GRCh38
NC_000007.13:g.99358602A>C , CM000669.1:g.99358602A>C	GRCh37
NC_000007.12:g.99196538A>C	NCBI36
NG_008421.1:g.28207T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1349T>G	ENSP00000337915.3:p.Phe450Cys
ENST00000651162.1:n.691T>G
ENST00000651514.1:c.1256T>G MANE Select	ENSP00000498939.1:p.Phe419Cys
ENST00000651783.1:c.797T>G	ENSP00000498924.1:p.Phe266Cys
ENST00000652018.1:c.1109T>G	ENSP00000498733.1:p.Phe370Cys
ENST00000336411.6:c.1256T>G	ENSP00000337915.2:p.Phe419Cys
ENST00000354593.6:c.806T>G	ENSP00000346607.2:p.Phe269Cys
NM_001202855.2:c.1253T>G	NP_001189784.1:p.Phe418Cys
NM_017460.5:c.1256T>G	NP_059488.2:p.Phe419Cys
XM_011515841.1:c.1349T>G	XP_011514143.1:p.Phe450Cys
XM_011515842.1:c.1346T>G	XP_011514144.1:p.Phe449Cys
NM_017460.6:c.1256T>G MANE Select	NP_059488.2:p.Phe419Cys
NM_001202855.3:c.1253T>G	NP_001189784.1:p.Phe418Cys