Canonical Allele Identifier: CA368372715

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99367389A>T (hg19) ; chr7:g.99769766A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769766A>T , CM000669.2:g.99769766A>T	GRCh38
NC_000007.13:g.99367389A>T , CM000669.1:g.99367389A>T	GRCh37
NC_000007.12:g.99205325A>T	NCBI36
NG_008421.1:g.19420T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+2T>A	ENSP00000337915.3:n.521+2T>A
ENST00000651514.1:c.521+2T>A MANE Select	ENSP00000498939.1:n.521+2T>A
ENST00000651783.1:c.58-1259T>A	ENSP00000498924.1:n.58-1259T>A
ENST00000652018.1:c.374+2T>A	ENSP00000498733.1:n.374+2T>A
ENST00000336411.6:c.521+2T>A	ENSP00000337915.2:n.521+2T>A
ENST00000354593.6:c.72-1264T>A	ENSP00000346607.2:n.72-1264T>A
ENST00000480043.1:n.420T>A
NM_001202855.2:c.521+2T>A	NP_001189784.1:n.521+2T>A
NM_017460.5:c.521+2T>A	NP_059488.2:n.521+2T>A
XM_011515841.1:c.521+2T>A	XP_011514143.1:n.521+2T>A
XM_011515842.1:c.521+2T>A	XP_011514144.1:n.521+2T>A
NM_017460.6:c.521+2T>A MANE Select	NP_059488.2:n.521+2T>A
NM_001202855.3:c.521+2T>A	NP_001189784.1:n.521+2T>A