Canonical Allele Identifier: CA2683985964

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99766995-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99766997del , CM000669.2:g.99766997del	GRCh38
NC_000007.13:g.99364620del , CM000669.1:g.99364620del	GRCh37
NC_000007.12:g.99202556del	NCBI36
NG_008421.1:g.22190del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.798+135del	ENSP00000337915.3:n.798+135del
ENST00000651162.1:n.233+135del
ENST00000651514.1:c.798+135del MANE Select	ENSP00000498939.1:n.798+135del
ENST00000651783.1:c.339+135del	ENSP00000498924.1:n.339+135del
ENST00000652018.1:c.651+135del	ENSP00000498733.1:n.651+135del
ENST00000336411.6:c.798+135del	ENSP00000337915.2:n.798+135del
ENST00000354593.6:c.348+135del	ENSP00000346607.2:n.348+135del
NM_001202855.2:c.795+135del	NP_001189784.1:n.795+135del
NM_017460.5:c.798+135del	NP_059488.2:n.798+135del
XM_011515841.1:c.798+135del	XP_011514143.1:n.798+135del
XM_011515842.1:c.795+135del	XP_011514144.1:n.795+135del
NM_017460.6:c.798+135del MANE Select	NP_059488.2:n.798+135del
NM_001202855.3:c.795+135del	NP_001189784.1:n.795+135del