Canonical Allele Identifier: CA844514379
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs1438008075

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768343_99768345del , CM000669.2:g.99768343_99768345del GRCh38
NC_000007.13:g.99365966_99365968del , CM000669.1:g.99365966_99365968del GRCh37
NC_000007.12:g.99203902_99203904del NCBI36
NG_008421.1:g.20845_20847del

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.670+13_670+15del ENSP00000337915.3:n.670+13_670+15del
ENST00000651514.1:c.670+13_670+15del MANE Select ENSP00000498939.1:n.670+13_670+15del
ENST00000651783.1:c.211+13_211+15del ENSP00000498924.1:n.211+13_211+15del
ENST00000652018.1:c.523+13_523+15del ENSP00000498733.1:n.523+13_523+15del
ENST00000336411.6:c.670+13_670+15del ENSP00000337915.2:n.670+13_670+15del
ENST00000354593.6:c.220+13_220+15del ENSP00000346607.2:n.220+13_220+15del
NM_001202855.2:c.670+13_670+15del NP_001189784.1:n.670+13_670+15del
NM_017460.5:c.670+13_670+15del NP_059488.2:n.670+13_670+15del
XM_011515841.1:c.670+13_670+15del XP_011514143.1:n.670+13_670+15del
XM_011515842.1:c.670+13_670+15del XP_011514144.1:n.670+13_670+15del
NM_017460.6:c.670+13_670+15del MANE Select NP_059488.2:n.670+13_670+15del
NM_001202855.3:c.670+13_670+15del NP_001189784.1:n.670+13_670+15del