Canonical Allele Identifier: CA368373255
Gene: CYP3A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99770123T>G , CM000669.2:g.99770123T>G GRCh38
NC_000007.13:g.99367746T>G , CM000669.1:g.99367746T>G GRCh37
NC_000007.12:g.99205682T>G NCBI36
NG_008421.1:g.19063A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.431A>C ENSP00000337915.3:p.Glu144Ala
ENST00000651514.1:c.431A>C MANE Select ENSP00000498939.1:p.Glu144Ala
ENST00000651783.1:c.58-1616A>C ENSP00000498924.1:n.58-1616A>C
ENST00000652018.1:c.284A>C ENSP00000498733.1:p.Glu95Ala
ENST00000336411.6:c.431A>C ENSP00000337915.2:p.Glu144Ala
ENST00000354593.6:c.72-1621A>C ENSP00000346607.2:n.72-1621A>C
ENST00000480043.1:n.328A>C
NM_001202855.2:c.431A>C NP_001189784.1:p.Glu144Ala
NM_017460.5:c.431A>C NP_059488.2:p.Glu144Ala
XM_011515841.1:c.431A>C XP_011514143.1:p.Glu144Ala
XM_011515842.1:c.431A>C XP_011514144.1:p.Glu144Ala
NM_017460.6:c.431A>C MANE Select NP_059488.2:p.Glu144Ala
NM_001202855.3:c.431A>C NP_001189784.1:p.Glu144Ala