Canonical Allele Identifier: CA576400238
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs1396698651

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99760827_99760830del , CM000669.2:g.99760827_99760830del GRCh38
NC_000007.13:g.99358450_99358453del , CM000669.1:g.99358450_99358453del GRCh37
NC_000007.12:g.99196386_99196389del NCBI36
NG_008421.1:g.28359_28362del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.1501_1504del ENSP00000337915.3:p.Glu501HisfsTer5
ENST00000651162.1:n.843_846del
ENST00000651514.1:c.1408_1411del MANE Select ENSP00000498939.1:p.Glu470HisfsTer5
ENST00000651783.1:c.949_952del ENSP00000498924.1:p.Glu317HisfsTer5
ENST00000652018.1:c.1261_1264del ENSP00000498733.1:p.Glu421HisfsTer5
ENST00000336411.6:c.1408_1411del ENSP00000337915.2:p.Glu470HisfsTer5
ENST00000354593.6:c.958_961del ENSP00000346607.2:p.Glu320HisfsTer5
NM_001202855.2:c.1405_1408del NP_001189784.1:p.Glu469HisfsTer5
NM_017460.5:c.1408_1411del NP_059488.2:p.Glu470HisfsTer5
XM_011515841.1:c.1501_1504del XP_011514143.1:p.Glu501HisfsTer5
XM_011515842.1:c.1498_1501del XP_011514144.1:p.Glu500HisfsTer5
NM_017460.6:c.1408_1411del MANE Select NP_059488.2:p.Glu470HisfsTer5
NM_001202855.3:c.1405_1408del NP_001189784.1:p.Glu469HisfsTer5