Canonical Allele Identifier: CA2777115515
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769390del , CM000669.2:g.99769390del GRCh38
NC_000007.13:g.99367013del , CM000669.1:g.99367013del GRCh37
NC_000007.12:g.99204949del NCBI36
NG_008421.1:g.19798del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.521+380del ENSP00000337915.3:n.521+380del
ENST00000651514.1:c.521+380del MANE Select ENSP00000498939.1:n.521+380del
ENST00000651783.1:c.58-881del ENSP00000498924.1:n.58-881del
ENST00000652018.1:c.374+380del ENSP00000498733.1:n.374+380del
ENST00000336411.6:c.521+380del ENSP00000337915.2:n.521+380del
ENST00000354593.6:c.72-886del ENSP00000346607.2:n.72-886del
NM_001202855.2:c.521+380del NP_001189784.1:n.521+380del
NM_017460.5:c.521+380del NP_059488.2:n.521+380del
XM_011515841.1:c.521+380del XP_011514143.1:n.521+380del
XM_011515842.1:c.521+380del XP_011514144.1:n.521+380del
NM_017460.6:c.521+380del MANE Select NP_059488.2:n.521+380del
NM_001202855.3:c.521+380del NP_001189784.1:n.521+380del