Canonical Allele Identifier: CA368368867

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99359697T>C (hg19) ; chr7:g.99762074T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762074T>C , CM000669.2:g.99762074T>C	GRCh38
NC_000007.13:g.99359697T>C , CM000669.1:g.99359697T>C	GRCh37
NC_000007.12:g.99197633T>C	NCBI36
NG_008421.1:g.27112A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1220A>G	ENSP00000337915.3:p.Tyr407Cys
ENST00000651162.1:n.655A>G
ENST00000651514.1:c.1220A>G MANE Select	ENSP00000498939.1:p.Tyr407Cys
ENST00000651783.1:c.761A>G	ENSP00000498924.1:p.Tyr254Cys
ENST00000652018.1:c.1073A>G	ENSP00000498733.1:p.Tyr358Cys
ENST00000336411.6:c.1220A>G	ENSP00000337915.2:p.Tyr407Cys
ENST00000354593.6:c.770A>G	ENSP00000346607.2:p.Tyr257Cys
NM_001202855.2:c.1217A>G	NP_001189784.1:p.Tyr406Cys
NM_017460.5:c.1220A>G	NP_059488.2:p.Tyr407Cys
XM_011515841.1:c.1220A>G	XP_011514143.1:p.Tyr407Cys
XM_011515842.1:c.1217A>G	XP_011514144.1:p.Tyr406Cys
NM_017460.6:c.1220A>G MANE Select	NP_059488.2:p.Tyr407Cys
NM_001202855.3:c.1217A>G	NP_001189784.1:p.Tyr406Cys