Canonical Allele Identifier: CA2578955197
Gene: CYP3A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768387del , CM000669.2:g.99768387del GRCh38
NC_000007.13:g.99366010del , CM000669.1:g.99366010del GRCh37
NC_000007.12:g.99203946del NCBI36
NG_008421.1:g.20801del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.639del ENSP00000337915.3:p.Phe213LeufsTer11
ENST00000651514.1:c.639del MANE Select ENSP00000498939.1:p.Phe213LeufsTer11
ENST00000651783.1:c.180del ENSP00000498924.1:p.Phe60LeufsTer11
ENST00000652018.1:c.492del ENSP00000498733.1:p.Phe164LeufsTer11
ENST00000336411.6:c.639del ENSP00000337915.2:p.Phe213LeufsTer11
ENST00000354593.6:c.189del ENSP00000346607.2:p.Phe63LeufsTer11
NM_001202855.2:c.639del NP_001189784.1:p.Phe213LeufsTer11
NM_017460.5:c.639del NP_059488.2:p.Phe213LeufsTer11
XM_011515841.1:c.639del XP_011514143.1:p.Phe213LeufsTer11
XM_011515842.1:c.639del XP_011514144.1:p.Phe213LeufsTer11
NM_017460.6:c.639del MANE Select NP_059488.2:p.Phe213LeufsTer11
NM_001202855.3:c.639del NP_001189784.1:p.Phe213LeufsTer11