Canonical Allele Identifier: CA368370175

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99767143-T-A
• MyVariant Identifiers: chr7:g.99364766T>A (hg19) ; chr7:g.99767143T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767143T>A , CM000669.2:g.99767143T>A	GRCh38
NC_000007.13:g.99364766T>A , CM000669.1:g.99364766T>A	GRCh37
NC_000007.12:g.99202702T>A	NCBI36
NG_008421.1:g.22043A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.786A>T	ENSP00000337915.3:p.Glu262Asp
ENST00000651162.1:n.221A>T
ENST00000651514.1:c.786A>T MANE Select	ENSP00000498939.1:p.Glu262Asp
ENST00000651783.1:c.327A>T	ENSP00000498924.1:p.Glu109Asp
ENST00000652018.1:c.639A>T	ENSP00000498733.1:p.Glu213Asp
ENST00000336411.6:c.786A>T	ENSP00000337915.2:p.Glu262Asp
ENST00000354593.6:c.336A>T	ENSP00000346607.2:p.Glu112Asp
NM_001202855.2:c.783A>T	NP_001189784.1:p.Glu261Asp
NM_017460.5:c.786A>T	NP_059488.2:p.Glu262Asp
XM_011515841.1:c.786A>T	XP_011514143.1:p.Glu262Asp
XM_011515842.1:c.783A>T	XP_011514144.1:p.Glu261Asp
NM_017460.6:c.786A>T MANE Select	NP_059488.2:p.Glu262Asp
NM_001202855.3:c.783A>T	NP_001189784.1:p.Glu261Asp