Canonical Allele Identifier: CA1729182240
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769873A= , CM000669.2:g.99769873A= GRCh38
NC_000007.13:g.99367496A= , CM000669.1:g.99367496A= GRCh37
NC_000007.12:g.99205432A= NCBI36
NG_008421.1:g.19313T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.433-17T= ENSP00000337915.3:n.433-17T=
ENST00000651514.1:c.433-17T= MANE Select ENSP00000498939.1:n.433-17T=
ENST00000651783.1:c.58-1366T= ENSP00000498924.1:n.58-1366T=
ENST00000652018.1:c.286-17T= ENSP00000498733.1:n.286-17T=
ENST00000336411.6:c.433-17T= ENSP00000337915.2:n.433-17T=
ENST00000354593.6:c.72-1371T= ENSP00000346607.2:n.72-1371T=
ENST00000480043.1:n.330-17T=
NM_001202855.2:c.433-17T= NP_001189784.1:n.433-17T=
NM_017460.5:c.433-17T= NP_059488.2:n.433-17T=
XM_011515841.1:c.433-17T= XP_011514143.1:n.433-17T=
XM_011515842.1:c.433-17T= XP_011514144.1:n.433-17T=
NM_017460.6:c.433-17T= MANE Select NP_059488.2:n.433-17T=
NM_001202855.3:c.433-17T= NP_001189784.1:n.433-17T=