Canonical Allele Identifier: CA1729176669
Gene: CYP3A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99760660C= , CM000669.2:g.99760660C= GRCh38
NC_000007.13:g.99358283C= , CM000669.1:g.99358283C= GRCh37
NC_000007.12:g.99196219C= NCBI36
NG_008421.1:g.28526G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.1509+159G= ENSP00000337915.3:n.1509+159G=
ENST00000651162.1:n.851+159G=
ENST00000651514.1:c.1416+159G= MANE Select ENSP00000498939.1:n.1416+159G=
ENST00000651783.1:c.957+159G= ENSP00000498924.1:n.957+159G=
ENST00000652018.1:c.1269+159G= ENSP00000498733.1:n.1269+159G=
ENST00000336411.6:c.1416+159G= ENSP00000337915.2:n.1416+159G=
ENST00000354593.6:c.966+159G= ENSP00000346607.2:n.966+159G=
NM_001202855.2:c.1413+159G= NP_001189784.1:n.1413+159G=
NM_017460.5:c.1416+159G= NP_059488.2:n.1416+159G=
XM_011515841.1:c.1509+159G= XP_011514143.1:n.1509+159G=
XM_011515842.1:c.1506+159G= XP_011514144.1:n.1506+159G=
NM_017460.6:c.1416+159G= MANE Select NP_059488.2:n.1416+159G=
NM_001202855.3:c.1413+159G= NP_001189784.1:n.1413+159G=
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