Canonical Allele Identifier: CA4369734

Gene: CYP3A4

Linked Data

• dbSNP Id: rs773580659
• ExAC: 7:99367388 TACTC / T
• gnomAD v2: 7-99367388-TACTC-T
• MyVariant Identifiers: chr7:g.99367389_99367392del (hg19) ; chr7:g.99769766_99769769del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769766_99769769del , CM000669.2:g.99769766_99769769del	GRCh38
NC_000007.13:g.99367389_99367392del , CM000669.1:g.99367389_99367392del	GRCh37
NC_000007.12:g.99205325_99205328del	NCBI36
NG_008421.1:g.19417_19420del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.520_521+2del
ENST00000651514.1:c.520_521+2del
ENST00000651783.1:c.58-1262_58-1259del	ENSP00000498924.1:n.58-1262_58-1259del
ENST00000652018.1:c.373_374+2del
ENST00000336411.6:c.520_521+2del
ENST00000354593.6:c.72-1267_72-1264del	ENSP00000346607.2:n.72-1267_72-1264del
ENST00000480043.1:n.417_420del
NM_001202855.2:c.520_521+2del
NM_017460.5:c.520_521+2del
XM_011515841.1:c.520_521+2del
XM_011515842.1:c.520_521+2del
NM_017460.6:c.520_521+2del
NM_001202855.3:c.520_521+2del