Canonical Allele Identifier: CA2578955177
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99767348del , CM000669.2:g.99767348del GRCh38
NC_000007.13:g.99364971del , CM000669.1:g.99364971del GRCh37
NC_000007.12:g.99202907del NCBI36
NG_008421.1:g.21839del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.671-89del ENSP00000337915.3:n.671-89del
ENST00000651162.1:n.106-89del
ENST00000651514.1:c.671-89del MANE Select ENSP00000498939.1:n.671-89del
ENST00000651783.1:c.212-89del ENSP00000498924.1:n.212-89del
ENST00000652018.1:c.524-89del ENSP00000498733.1:n.524-89del
ENST00000336411.6:c.671-89del ENSP00000337915.2:n.671-89del
ENST00000354593.6:c.221-89del ENSP00000346607.2:n.221-89del
NM_001202855.2:c.671-92del NP_001189784.1:n.671-92del
NM_017460.5:c.671-89del NP_059488.2:n.671-89del
XM_011515841.1:c.671-89del XP_011514143.1:n.671-89del
XM_011515842.1:c.671-92del XP_011514144.1:n.671-92del
NM_017460.6:c.671-89del MANE Select NP_059488.2:n.671-89del
NM_001202855.3:c.671-92del NP_001189784.1:n.671-92del