Canonical Allele Identifier: CA844515655

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1282357017
• gnomAD v3: 7-99770050-A-ATC
• gnomAD v4: 7-99770050-A-ATC
• MyVariant Identifiers: chr7:g.99367673_99367674insTC (hg19) ; chr7:g.99770050_99770051insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770052_99770053dup , CM000669.2:g.99770052_99770053dup	GRCh38
NC_000007.13:g.99367675_99367676dup , CM000669.1:g.99367675_99367676dup	GRCh37
NC_000007.12:g.99205611_99205612dup	NCBI36
NG_008421.1:g.19134_19135dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.432+70_432+71dup	ENSP00000337915.3:n.432+70_432+71dup
ENST00000651514.1:c.432+70_432+71dup MANE Select	ENSP00000498939.1:n.432+70_432+71dup
ENST00000651783.1:c.58-1545_58-1544dup	ENSP00000498924.1:n.58-1545_58-1544dup
ENST00000652018.1:c.285+70_285+71dup	ENSP00000498733.1:n.285+70_285+71dup
ENST00000336411.6:c.432+70_432+71dup	ENSP00000337915.2:n.432+70_432+71dup
ENST00000354593.6:c.72-1550_72-1549dup	ENSP00000346607.2:n.72-1550_72-1549dup
ENST00000480043.1:n.329+70_329+71dup
NM_001202855.2:c.432+70_432+71dup	NP_001189784.1:n.432+70_432+71dup
NM_017460.5:c.432+70_432+71dup	NP_059488.2:n.432+70_432+71dup
XM_011515841.1:c.432+70_432+71dup	XP_011514143.1:n.432+70_432+71dup
XM_011515842.1:c.432+70_432+71dup	XP_011514144.1:n.432+70_432+71dup
NM_017460.6:c.432+70_432+71dup MANE Select	NP_059488.2:n.432+70_432+71dup
NM_001202855.3:c.432+70_432+71dup	NP_001189784.1:n.432+70_432+71dup