Canonical Allele Identifier: CA368373015
Gene: CYP3A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769826C>A , CM000669.2:g.99769826C>A GRCh38
NC_000007.13:g.99367449C>A , CM000669.1:g.99367449C>A GRCh37
NC_000007.12:g.99205385C>A NCBI36
NG_008421.1:g.19360G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.463G>T ENSP00000337915.3:p.Val155Leu
ENST00000651514.1:c.463G>T MANE Select ENSP00000498939.1:p.Val155Leu
ENST00000651783.1:c.58-1319G>T ENSP00000498924.1:n.58-1319G>T
ENST00000652018.1:c.316G>T ENSP00000498733.1:p.Val106Leu
ENST00000336411.6:c.463G>T ENSP00000337915.2:p.Val155Leu
ENST00000354593.6:c.72-1324G>T ENSP00000346607.2:n.72-1324G>T
ENST00000480043.1:n.360G>T
NM_001202855.2:c.463G>T NP_001189784.1:p.Val155Leu
NM_017460.5:c.463G>T NP_059488.2:p.Val155Leu
XM_011515841.1:c.463G>T XP_011514143.1:p.Val155Leu
XM_011515842.1:c.463G>T XP_011514144.1:p.Val155Leu
NM_017460.6:c.463G>T MANE Select NP_059488.2:p.Val155Leu
NM_001202855.3:c.463G>T NP_001189784.1:p.Val155Leu