Canonical Allele Identifier: CA1729179944
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99767150C= , CM000669.2:g.99767150C= GRCh38
NC_000007.13:g.99364773C= , CM000669.1:g.99364773C= GRCh37
NC_000007.12:g.99202709C= NCBI36
NG_008421.1:g.22036G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.779G= ENSP00000337915.3:p.Arg260=
ENST00000651162.1:n.214G=
ENST00000651514.1:c.779G= MANE Select ENSP00000498939.1:p.Arg260=
ENST00000651783.1:c.320G= ENSP00000498924.1:p.Arg107=
ENST00000652018.1:c.632G= ENSP00000498733.1:p.Arg211=
ENST00000336411.6:c.779G= ENSP00000337915.2:p.Arg260=
ENST00000354593.6:c.329G= ENSP00000346607.2:p.Arg110=
NM_001202855.2:c.776G= NP_001189784.1:p.Arg259=
NM_017460.5:c.779G= NP_059488.2:p.Arg260=
XM_011515841.1:c.779G= XP_011514143.1:p.Arg260=
XM_011515842.1:c.776G= XP_011514144.1:p.Arg259=
NM_017460.6:c.779G= MANE Select NP_059488.2:p.Arg260=
NM_001202855.3:c.776G= NP_001189784.1:p.Arg259=