Canonical Allele Identifier: CA368374716
Community Standard Title: NM_017460.6(CYP3A4):c.44T>A (p.Leu15Gln)
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99784038A>T , CM000669.2:g.99784038A>T GRCh38
NC_000007.13:g.99381661A>T , CM000669.1:g.99381661A>T GRCh37
NC_000007.12:g.99219597A>T NCBI36
NG_008421.1:g.5148T>A

Transcript Alleles

HGVS Amino-acid Change
NM_017460.6:c.44T>A MANE Select NP_059488.2:p.Leu15Gln
ENST00000651514.1:c.44T>A MANE Select ENSP00000498939.1:p.Leu15Gln
NM_001202855.2:c.44T>A NP_001189784.1:p.Leu15Gln
NM_001202855.3:c.44T>A NP_001189784.1:p.Leu15Gln
NM_017460.5:c.44T>A NP_059488.2:p.Leu15Gln
ENST00000336411.6:c.44T>A ENSP00000337915.2:p.Leu15Gln
ENST00000336411.7:c.44T>A ENSP00000337915.3:p.Leu15Gln
ENST00000354593.6:c.44T>A ENSP00000346607.2:p.Leu15Gln
ENST00000415003.1:c.44T>A ENSP00000397208.1:p.Leu15Gln
ENST00000652018.1:c.44T>A ENSP00000498733.1:p.Leu15Gln
XM_011515841.1:c.44T>A XP_011514143.1:p.Leu15Gln
XM_011515842.1:c.44T>A XP_011514144.1:p.Leu15Gln