Canonical Allele Identifier: CA2683986529

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99769996-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769996G>T , CM000669.2:g.99769996G>T	GRCh38
NC_000007.13:g.99367619G>T , CM000669.1:g.99367619G>T	GRCh37
NC_000007.12:g.99205555G>T	NCBI36
NG_008421.1:g.19190C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.432+126C>A	ENSP00000337915.3:n.432+126C>A
ENST00000651514.1:c.432+126C>A MANE Select	ENSP00000498939.1:n.432+126C>A
ENST00000651783.1:c.58-1489C>A	ENSP00000498924.1:n.58-1489C>A
ENST00000652018.1:c.285+126C>A	ENSP00000498733.1:n.285+126C>A
ENST00000336411.6:c.432+126C>A	ENSP00000337915.2:n.432+126C>A
ENST00000354593.6:c.72-1494C>A	ENSP00000346607.2:n.72-1494C>A
ENST00000480043.1:n.329+126C>A
NM_001202855.2:c.432+126C>A	NP_001189784.1:n.432+126C>A
NM_017460.5:c.432+126C>A	NP_059488.2:n.432+126C>A
XM_011515841.1:c.432+126C>A	XP_011514143.1:n.432+126C>A
XM_011515842.1:c.432+126C>A	XP_011514144.1:n.432+126C>A
NM_017460.6:c.432+126C>A MANE Select	NP_059488.2:n.432+126C>A
NM_001202855.3:c.432+126C>A	NP_001189784.1:n.432+126C>A