Canonical Allele Identifier: CA368373160
Gene: CYP3A4 HGNC NCBI

Linked Data

gnomAD v4: 7-99769853-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769853C>A , CM000669.2:g.99769853C>A GRCh38
NC_000007.13:g.99367476C>A , CM000669.1:g.99367476C>A GRCh37
NC_000007.12:g.99205412C>A NCBI36
NG_008421.1:g.19333G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.436G>T ENSP00000337915.3:p.Val146Phe
ENST00000651514.1:c.436G>T MANE Select ENSP00000498939.1:p.Val146Phe
ENST00000651783.1:c.58-1346G>T ENSP00000498924.1:n.58-1346G>T
ENST00000652018.1:c.289G>T ENSP00000498733.1:p.Val97Phe
ENST00000336411.6:c.436G>T ENSP00000337915.2:p.Val146Phe
ENST00000354593.6:c.72-1351G>T ENSP00000346607.2:n.72-1351G>T
ENST00000480043.1:n.333G>T
NM_001202855.2:c.436G>T NP_001189784.1:p.Val146Phe
NM_017460.5:c.436G>T NP_059488.2:p.Val146Phe
XM_011515841.1:c.436G>T XP_011514143.1:p.Val146Phe
XM_011515842.1:c.436G>T XP_011514144.1:p.Val146Phe
NM_017460.6:c.436G>T MANE Select NP_059488.2:p.Val146Phe
NM_001202855.3:c.436G>T NP_001189784.1:p.Val146Phe