Canonical Allele Identifier: CA163153830

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1015393363
• gnomAD v3: 7-99769983-CATAAAG-C
• gnomAD v4: 7-99769983-CATAAAG-C
• MyVariant Identifiers: chr7:g.99367607_99367612del (hg19) ; chr7:g.99769984_99769989del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769989_99769994del , CM000669.2:g.99769989_99769994del	GRCh38
NC_000007.13:g.99367612_99367617del , CM000669.1:g.99367612_99367617del	GRCh37
NC_000007.12:g.99205548_99205553del	NCBI36
NG_008421.1:g.19197_19202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.433-133_433-128del	ENSP00000337915.3:n.433-133_433-128del
ENST00000651514.1:c.433-133_433-128del MANE Select	ENSP00000498939.1:n.433-133_433-128del
ENST00000651783.1:c.58-1482_58-1477del	ENSP00000498924.1:n.58-1482_58-1477del
ENST00000652018.1:c.286-133_286-128del	ENSP00000498733.1:n.286-133_286-128del
ENST00000336411.6:c.433-133_433-128del	ENSP00000337915.2:n.433-133_433-128del
ENST00000354593.6:c.72-1487_72-1482del	ENSP00000346607.2:n.72-1487_72-1482del
ENST00000480043.1:n.330-133_330-128del
NM_001202855.2:c.433-133_433-128del	NP_001189784.1:n.433-133_433-128del
NM_017460.5:c.433-133_433-128del	NP_059488.2:n.433-133_433-128del
XM_011515841.1:c.433-133_433-128del	XP_011514143.1:n.433-133_433-128del
XM_011515842.1:c.433-133_433-128del	XP_011514144.1:n.433-133_433-128del
NM_017460.6:c.433-133_433-128del MANE Select	NP_059488.2:n.433-133_433-128del
NM_001202855.3:c.433-133_433-128del	NP_001189784.1:n.433-133_433-128del