Canonical Allele Identifier: CA2537912214
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99767078del , CM000669.2:g.99767078del GRCh38
NC_000007.13:g.99364701del , CM000669.1:g.99364701del GRCh37
NC_000007.12:g.99202637del NCBI36
NG_008421.1:g.22108del

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.798+53del ENSP00000337915.3:n.798+53del
ENST00000651162.1:n.233+53del
ENST00000651514.1:c.798+53del MANE Select ENSP00000498939.1:n.798+53del
ENST00000651783.1:c.339+53del ENSP00000498924.1:n.339+53del
ENST00000652018.1:c.651+53del ENSP00000498733.1:n.651+53del
ENST00000336411.6:c.798+53del ENSP00000337915.2:n.798+53del
ENST00000354593.6:c.348+53del ENSP00000346607.2:n.348+53del
NM_001202855.2:c.795+53del NP_001189784.1:n.795+53del
NM_017460.5:c.798+53del NP_059488.2:n.798+53del
XM_011515841.1:c.798+53del XP_011514143.1:n.798+53del
XM_011515842.1:c.795+53del XP_011514144.1:n.795+53del
NM_017460.6:c.798+53del MANE Select NP_059488.2:n.798+53del
NM_001202855.3:c.795+53del NP_001189784.1:n.795+53del