Canonical Allele Identifier: CA368368970

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99762106-A-C
• MyVariant Identifiers: chr7:g.99359729A>C (hg19) ; chr7:g.99762106A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762106A>C , CM000669.2:g.99762106A>C	GRCh38
NC_000007.13:g.99359729A>C , CM000669.1:g.99359729A>C	GRCh37
NC_000007.12:g.99197665A>C	NCBI36
NG_008421.1:g.27080T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1188T>G	ENSP00000337915.3:p.Ile396Met
ENST00000651162.1:n.623T>G
ENST00000651514.1:c.1188T>G MANE Select	ENSP00000498939.1:p.Ile396Met
ENST00000651783.1:c.729T>G	ENSP00000498924.1:p.Ile243Met
ENST00000652018.1:c.1041T>G	ENSP00000498733.1:p.Ile347Met
ENST00000336411.6:c.1188T>G	ENSP00000337915.2:p.Ile396Met
ENST00000354593.6:c.738T>G	ENSP00000346607.2:p.Ile246Met
NM_001202855.2:c.1185T>G	NP_001189784.1:p.Ile395Met
NM_017460.5:c.1188T>G	NP_059488.2:p.Ile396Met
XM_011515841.1:c.1188T>G	XP_011514143.1:p.Ile396Met
XM_011515842.1:c.1185T>G	XP_011514144.1:p.Ile395Met
NM_017460.6:c.1188T>G MANE Select	NP_059488.2:p.Ile396Met
NM_001202855.3:c.1185T>G	NP_001189784.1:p.Ile395Met