Canonical Allele Identifier: CA456687187

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99762151-A-C
• MyVariant Identifiers: chr7:g.99359774A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762151A>C , CM000669.2:g.99762151A>C	GRCh38
NC_000007.13:g.99359774A>C , CM000669.1:g.99359774A>C	GRCh37
NC_000007.12:g.99197710A>C	NCBI36
NG_008421.1:g.27035T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1143T>G	ENSP00000337915.3:p.Val381=
ENST00000651162.1:n.578T>G
ENST00000651514.1:c.1143T>G MANE Select	ENSP00000498939.1:p.Val381=
ENST00000651783.1:c.684T>G	ENSP00000498924.1:p.Val228=
ENST00000652018.1:c.996T>G	ENSP00000498733.1:p.Val332=
ENST00000336411.6:c.1143T>G	ENSP00000337915.2:p.Val381=
ENST00000354593.6:c.693T>G	ENSP00000346607.2:p.Val231=
NM_001202855.2:c.1140T>G	NP_001189784.1:p.Val380=
NM_017460.5:c.1143T>G	NP_059488.2:p.Val381=
XM_011515841.1:c.1143T>G	XP_011514143.1:p.Val381=
XM_011515842.1:c.1140T>G	XP_011514144.1:p.Val380=
NM_017460.6:c.1143T>G MANE Select	NP_059488.2:p.Val381=
NM_001202855.3:c.1140T>G	NP_001189784.1:p.Val380=