Canonical Allele Identifier: CA1104978955

Gene: CYP3A4

Linked Data

• gnomAD v3: 7-99769337-GA-G
• gnomAD v4: 7-99769337-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769344del , CM000669.2:g.99769344del	GRCh38
NC_000007.13:g.99366967del , CM000669.1:g.99366967del	GRCh37
NC_000007.12:g.99204903del	NCBI36
NG_008421.1:g.19848del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+430del	ENSP00000337915.3:n.521+430del
ENST00000651514.1:c.521+430del MANE Select	ENSP00000498939.1:n.521+430del
ENST00000651783.1:c.58-831del	ENSP00000498924.1:n.58-831del
ENST00000652018.1:c.374+430del	ENSP00000498733.1:n.374+430del
ENST00000336411.6:c.521+430del	ENSP00000337915.2:n.521+430del
ENST00000354593.6:c.72-836del	ENSP00000346607.2:n.72-836del
NM_001202855.2:c.521+430del	NP_001189784.1:n.521+430del
NM_017460.5:c.521+430del	NP_059488.2:n.521+430del
XM_011515841.1:c.521+430del	XP_011514143.1:n.521+430del
XM_011515842.1:c.521+430del	XP_011514144.1:n.521+430del
NM_017460.6:c.521+430del MANE Select	NP_059488.2:n.521+430del
NM_001202855.3:c.521+430del	NP_001189784.1:n.521+430del