Canonical Allele Identifier: CA368374077
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99772622T>A , CM000669.2:g.99772622T>A GRCh38
NC_000007.13:g.99370245T>A , CM000669.1:g.99370245T>A GRCh37
NC_000007.12:g.99208181T>A NCBI36
NG_008421.1:g.16564A>T

Transcript Alleles

HGVS Amino-acid Change
NM_017460.6:c.286A>T MANE Select NP_059488.2:p.Lys96Ter
ENST00000651514.1:c.286A>T MANE Select ENSP00000498939.1:p.Lys96Ter
NM_001202855.2:c.286A>T NP_001189784.1:p.Lys96Ter
NM_001202855.3:c.286A>T NP_001189784.1:p.Lys96Ter
NM_017460.5:c.286A>T NP_059488.2:p.Lys96Ter
ENST00000336411.6:c.286A>T ENSP00000337915.2:p.Lys96Ter
ENST00000336411.7:c.286A>T ENSP00000337915.3:p.Lys96Ter
ENST00000354593.6:c.72-4120A>T ENSP00000346607.2:n.72-4120A>T
ENST00000415003.1:c.325A>T ENSP00000397208.1:p.Lys109Ter
ENST00000480043.1:n.183A>T
ENST00000651783.1:c.58-4115A>T ENSP00000498924.1:n.58-4115A>T
ENST00000652018.1:c.139A>T ENSP00000498733.1:p.Lys47Ter
XM_011515841.1:c.286A>T XP_011514143.1:p.Lys96Ter
XM_011515842.1:c.286A>T XP_011514144.1:p.Lys96Ter