Canonical Allele Identifier: CA2683986455

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99769707-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769708del , CM000669.2:g.99769708del	GRCh38
NC_000007.13:g.99367331del , CM000669.1:g.99367331del	GRCh37
NC_000007.12:g.99205267del	NCBI36
NG_008421.1:g.19478del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+60del	ENSP00000337915.3:n.521+60del
ENST00000651514.1:c.521+60del MANE Select	ENSP00000498939.1:n.521+60del
ENST00000651783.1:c.58-1201del	ENSP00000498924.1:n.58-1201del
ENST00000652018.1:c.374+60del	ENSP00000498733.1:n.374+60del
ENST00000336411.6:c.521+60del	ENSP00000337915.2:n.521+60del
ENST00000354593.6:c.72-1206del	ENSP00000346607.2:n.72-1206del
ENST00000480043.1:n.478del
NM_001202855.2:c.521+60del	NP_001189784.1:n.521+60del
NM_017460.5:c.521+60del	NP_059488.2:n.521+60del
XM_011515841.1:c.521+60del	XP_011514143.1:n.521+60del
XM_011515842.1:c.521+60del	XP_011514144.1:n.521+60del
NM_017460.6:c.521+60del MANE Select	NP_059488.2:n.521+60del
NM_001202855.3:c.521+60del	NP_001189784.1:n.521+60del