Canonical Allele Identifier: CA1729176713
Gene: CYP3A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99760791A= , CM000669.2:g.99760791A= GRCh38
NC_000007.13:g.99358414A= , CM000669.1:g.99358414A= GRCh37
NC_000007.12:g.99196350A= NCBI36
NG_008421.1:g.28395T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.1509+28T= ENSP00000337915.3:n.1509+28T=
ENST00000651162.1:n.851+28T=
ENST00000651514.1:c.1416+28T= MANE Select ENSP00000498939.1:n.1416+28T=
ENST00000651783.1:c.957+28T= ENSP00000498924.1:n.957+28T=
ENST00000652018.1:c.1269+28T= ENSP00000498733.1:n.1269+28T=
ENST00000336411.6:c.1416+28T= ENSP00000337915.2:n.1416+28T=
ENST00000354593.6:c.966+28T= ENSP00000346607.2:n.966+28T=
NM_001202855.2:c.1413+28T= NP_001189784.1:n.1413+28T=
NM_017460.5:c.1416+28T= NP_059488.2:n.1416+28T=
XM_011515841.1:c.1509+28T= XP_011514143.1:n.1509+28T=
XM_011515842.1:c.1506+28T= XP_011514144.1:n.1506+28T=
NM_017460.6:c.1416+28T= MANE Select NP_059488.2:n.1416+28T=
NM_001202855.3:c.1413+28T= NP_001189784.1:n.1413+28T=
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