Canonical Allele Identifier: CA368368607

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358529A>C (hg19) ; chr7:g.99760906A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760906A>C , CM000669.2:g.99760906A>C	GRCh38
NC_000007.13:g.99358529A>C , CM000669.1:g.99358529A>C	GRCh37
NC_000007.12:g.99196465A>C	NCBI36
NG_008421.1:g.28280T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1422T>G	ENSP00000337915.3:p.Ile474Met
ENST00000651162.1:n.764T>G
ENST00000651514.1:c.1329T>G MANE Select	ENSP00000498939.1:p.Ile443Met
ENST00000651783.1:c.870T>G	ENSP00000498924.1:p.Ile290Met
ENST00000652018.1:c.1182T>G	ENSP00000498733.1:p.Ile394Met
ENST00000336411.6:c.1329T>G	ENSP00000337915.2:p.Ile443Met
ENST00000354593.6:c.879T>G	ENSP00000346607.2:p.Ile293Met
NM_001202855.2:c.1326T>G	NP_001189784.1:p.Ile442Met
NM_017460.5:c.1329T>G	NP_059488.2:p.Ile443Met
XM_011515841.1:c.1422T>G	XP_011514143.1:p.Ile474Met
XM_011515842.1:c.1419T>G	XP_011514144.1:p.Ile473Met
NM_017460.6:c.1329T>G MANE Select	NP_059488.2:p.Ile443Met
NM_001202855.3:c.1326T>G	NP_001189784.1:p.Ile442Met