Canonical Allele Identifier: CA368369941
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99764003A>C , CM000669.2:g.99764003A>C GRCh38
NC_000007.13:g.99361626A>C , CM000669.1:g.99361626A>C GRCh37
NC_000007.12:g.99199562A>C NCBI36
NG_008421.1:g.25183T>G

Transcript Alleles

HGVS Amino-acid Change
NM_017460.6:c.878T>G MANE Select NP_059488.2:p.Leu293Arg
ENST00000651514.1:c.878T>G MANE Select ENSP00000498939.1:p.Leu293Arg
NM_001202855.2:c.875T>G NP_001189784.1:p.Leu292Arg
NM_001202855.3:c.875T>G NP_001189784.1:p.Leu292Arg
NM_017460.5:c.878T>G NP_059488.2:p.Leu293Arg
ENST00000336411.6:c.878T>G ENSP00000337915.2:p.Leu293Arg
ENST00000336411.7:c.878T>G ENSP00000337915.3:p.Leu293Arg
ENST00000354593.6:c.428T>G ENSP00000346607.2:p.Leu143Arg
ENST00000651162.1:n.313T>G
ENST00000651783.1:c.419T>G ENSP00000498924.1:p.Leu140Arg
ENST00000652018.1:c.731T>G ENSP00000498733.1:p.Leu244Arg
XM_011515841.1:c.878T>G XP_011514143.1:p.Leu293Arg
XM_011515842.1:c.875T>G XP_011514144.1:p.Leu292Arg