Canonical Allele Identifier: CA1729179838
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99767034C= , CM000669.2:g.99767034C= GRCh38
NC_000007.13:g.99364657C= , CM000669.1:g.99364657C= GRCh37
NC_000007.12:g.99202593C= NCBI36
NG_008421.1:g.22152G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.798+97G= ENSP00000337915.3:n.798+97G=
ENST00000651162.1:n.233+97G=
ENST00000651514.1:c.798+97G= MANE Select ENSP00000498939.1:n.798+97G=
ENST00000651783.1:c.339+97G= ENSP00000498924.1:n.339+97G=
ENST00000652018.1:c.651+97G= ENSP00000498733.1:n.651+97G=
ENST00000336411.6:c.798+97G= ENSP00000337915.2:n.798+97G=
ENST00000354593.6:c.348+97G= ENSP00000346607.2:n.348+97G=
NM_001202855.2:c.795+97G= NP_001189784.1:n.795+97G=
NM_017460.5:c.798+97G= NP_059488.2:n.798+97G=
XM_011515841.1:c.798+97G= XP_011514143.1:n.798+97G=
XM_011515842.1:c.795+97G= XP_011514144.1:n.795+97G=
NM_017460.6:c.798+97G= MANE Select NP_059488.2:n.798+97G=
NM_001202855.3:c.795+97G= NP_001189784.1:n.795+97G=