Canonical Allele Identifier: CA1729182458
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99770125C= , CM000669.2:g.99770125C= GRCh38
NC_000007.13:g.99367748C= , CM000669.1:g.99367748C= GRCh37
NC_000007.12:g.99205684C= NCBI36
NG_008421.1:g.19061G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.429G= ENSP00000337915.3:p.Lys143=
ENST00000651514.1:c.429G= MANE Select ENSP00000498939.1:p.Lys143=
ENST00000651783.1:c.58-1618G= ENSP00000498924.1:n.58-1618G=
ENST00000652018.1:c.282G= ENSP00000498733.1:p.Lys94=
ENST00000336411.6:c.429G= ENSP00000337915.2:p.Lys143=
ENST00000354593.6:c.72-1623G= ENSP00000346607.2:n.72-1623G=
ENST00000480043.1:n.326G=
NM_001202855.2:c.429G= NP_001189784.1:p.Lys143=
NM_017460.5:c.429G= NP_059488.2:p.Lys143=
XM_011515841.1:c.429G= XP_011514143.1:p.Lys143=
XM_011515842.1:c.429G= XP_011514144.1:p.Lys143=
NM_017460.6:c.429G= MANE Select NP_059488.2:p.Lys143=
NM_001202855.3:c.429G= NP_001189784.1:p.Lys143=