Canonical Allele Identifier: CA2683986148

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99768252-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768254_99768255del , CM000669.2:g.99768254_99768255del	GRCh38
NC_000007.13:g.99365877_99365878del , CM000669.1:g.99365877_99365878del	GRCh37
NC_000007.12:g.99203813_99203814del	NCBI36
NG_008421.1:g.20932_20933del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.670+100_670+101del	ENSP00000337915.3:n.670+100_670+101del
ENST00000651514.1:c.670+100_670+101del MANE Select	ENSP00000498939.1:n.670+100_670+101del
ENST00000651783.1:c.211+100_211+101del	ENSP00000498924.1:n.211+100_211+101del
ENST00000652018.1:c.523+100_523+101del	ENSP00000498733.1:n.523+100_523+101del
ENST00000336411.6:c.670+100_670+101del	ENSP00000337915.2:n.670+100_670+101del
ENST00000354593.6:c.220+100_220+101del	ENSP00000346607.2:n.220+100_220+101del
NM_001202855.2:c.670+100_670+101del	NP_001189784.1:n.670+100_670+101del
NM_017460.5:c.670+100_670+101del	NP_059488.2:n.670+100_670+101del
XM_011515841.1:c.670+100_670+101del	XP_011514143.1:n.670+100_670+101del
XM_011515842.1:c.670+100_670+101del	XP_011514144.1:n.670+100_670+101del
NM_017460.6:c.670+100_670+101del MANE Select	NP_059488.2:n.670+100_670+101del
NM_001202855.3:c.670+100_670+101del	NP_001189784.1:n.670+100_670+101del