Canonical Allele Identifier: CA368368689

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99760943-A-C
• MyVariant Identifiers: chr7:g.99358566A>C (hg19) ; chr7:g.99760943A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760943A>C , CM000669.2:g.99760943A>C	GRCh38
NC_000007.13:g.99358566A>C , CM000669.1:g.99358566A>C	GRCh37
NC_000007.12:g.99196502A>C	NCBI36
NG_008421.1:g.28243T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1385T>G	ENSP00000337915.3:p.Ile462Arg
ENST00000651162.1:n.727T>G
ENST00000651514.1:c.1292T>G MANE Select	ENSP00000498939.1:p.Ile431Arg
ENST00000651783.1:c.833T>G	ENSP00000498924.1:p.Ile278Arg
ENST00000652018.1:c.1145T>G	ENSP00000498733.1:p.Ile382Arg
ENST00000336411.6:c.1292T>G	ENSP00000337915.2:p.Ile431Arg
ENST00000354593.6:c.842T>G	ENSP00000346607.2:p.Ile281Arg
NM_001202855.2:c.1289T>G	NP_001189784.1:p.Ile430Arg
NM_017460.5:c.1292T>G	NP_059488.2:p.Ile431Arg
XM_011515841.1:c.1385T>G	XP_011514143.1:p.Ile462Arg
XM_011515842.1:c.1382T>G	XP_011514144.1:p.Ile461Arg
NM_017460.6:c.1292T>G MANE Select	NP_059488.2:p.Ile431Arg
NM_001202855.3:c.1289T>G	NP_001189784.1:p.Ile430Arg