Canonical Allele Identifier: CA1729181763

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815568496

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769366_99769367del , CM000669.2:g.99769366_99769367del	GRCh38
NC_000007.13:g.99366989_99366990del , CM000669.1:g.99366989_99366990del	GRCh37
NC_000007.12:g.99204925_99204926del	NCBI36
NG_008421.1:g.19820_19821del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+402_521+403del	ENSP00000337915.3:n.521+402_521+403del
ENST00000651514.1:c.521+402_521+403del MANE Select	ENSP00000498939.1:n.521+402_521+403del
ENST00000651783.1:c.58-859_58-858del	ENSP00000498924.1:n.58-859_58-858del
ENST00000652018.1:c.374+402_374+403del	ENSP00000498733.1:n.374+402_374+403del
ENST00000336411.6:c.521+402_521+403del	ENSP00000337915.2:n.521+402_521+403del
ENST00000354593.6:c.72-864_72-863del	ENSP00000346607.2:n.72-864_72-863del
NM_001202855.2:c.521+402_521+403del	NP_001189784.1:n.521+402_521+403del
NM_017460.5:c.521+402_521+403del	NP_059488.2:n.521+402_521+403del
XM_011515841.1:c.521+402_521+403del	XP_011514143.1:n.521+402_521+403del
XM_011515842.1:c.521+402_521+403del	XP_011514144.1:n.521+402_521+403del
NM_017460.6:c.521+402_521+403del MANE Select	NP_059488.2:n.521+402_521+403del
NM_001202855.3:c.521+402_521+403del	NP_001189784.1:n.521+402_521+403del