Canonical Allele Identifier: CA1729182078
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769707A= , CM000669.2:g.99769707A= GRCh38
NC_000007.13:g.99367330A= , CM000669.1:g.99367330A= GRCh37
NC_000007.12:g.99205266A= NCBI36
NG_008421.1:g.19479T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.521+61T= ENSP00000337915.3:n.521+61T=
ENST00000651514.1:c.521+61T= MANE Select ENSP00000498939.1:n.521+61T=
ENST00000651783.1:c.58-1200T= ENSP00000498924.1:n.58-1200T=
ENST00000652018.1:c.374+61T= ENSP00000498733.1:n.374+61T=
ENST00000336411.6:c.521+61T= ENSP00000337915.2:n.521+61T=
ENST00000354593.6:c.72-1205T= ENSP00000346607.2:n.72-1205T=
ENST00000480043.1:n.479T=
NM_001202855.2:c.521+61T= NP_001189784.1:n.521+61T=
NM_017460.5:c.521+61T= NP_059488.2:n.521+61T=
XM_011515841.1:c.521+61T= XP_011514143.1:n.521+61T=
XM_011515842.1:c.521+61T= XP_011514144.1:n.521+61T=
NM_017460.6:c.521+61T= MANE Select NP_059488.2:n.521+61T=
NM_001202855.3:c.521+61T= NP_001189784.1:n.521+61T=