Canonical Allele Identifier: CA368373333

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99770137-A-T
• MyVariant Identifiers: chr7:g.99367760A>T (hg19) ; chr7:g.99770137A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770137A>T , CM000669.2:g.99770137A>T	GRCh38
NC_000007.13:g.99367760A>T , CM000669.1:g.99367760A>T	GRCh37
NC_000007.12:g.99205696A>T	NCBI36
NG_008421.1:g.19049T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.417T>A	ENSP00000337915.3:p.Ser139Arg
ENST00000651514.1:c.417T>A MANE Select	ENSP00000498939.1:p.Ser139Arg
ENST00000651783.1:c.58-1630T>A	ENSP00000498924.1:n.58-1630T>A
ENST00000652018.1:c.270T>A	ENSP00000498733.1:p.Ser90Arg
ENST00000336411.6:c.417T>A	ENSP00000337915.2:p.Ser139Arg
ENST00000354593.6:c.72-1635T>A	ENSP00000346607.2:n.72-1635T>A
ENST00000415003.1:c.456T>A	ENSP00000397208.1:p.Ser152Arg
ENST00000480043.1:n.314T>A
NM_001202855.2:c.417T>A	NP_001189784.1:p.Ser139Arg
NM_017460.5:c.417T>A	NP_059488.2:p.Ser139Arg
XM_011515841.1:c.417T>A	XP_011514143.1:p.Ser139Arg
XM_011515842.1:c.417T>A	XP_011514144.1:p.Ser139Arg
NM_017460.6:c.417T>A MANE Select	NP_059488.2:p.Ser139Arg
NM_001202855.3:c.417T>A	NP_001189784.1:p.Ser139Arg