Canonical Allele Identifier: CA2683986529
Gene: CYP3A4 HGNC NCBI

Linked Data

gnomAD v4: 7-99769996-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769996G>T , CM000669.2:g.99769996G>T GRCh38
NC_000007.13:g.99367619G>T , CM000669.1:g.99367619G>T GRCh37
NC_000007.12:g.99205555G>T NCBI36
NG_008421.1:g.19190C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.432+126C>A ENSP00000337915.3:n.432+126C>A
ENST00000651514.1:c.432+126C>A MANE Select ENSP00000498939.1:n.432+126C>A
ENST00000651783.1:c.58-1489C>A ENSP00000498924.1:n.58-1489C>A
ENST00000652018.1:c.285+126C>A ENSP00000498733.1:n.285+126C>A
ENST00000336411.6:c.432+126C>A ENSP00000337915.2:n.432+126C>A
ENST00000354593.6:c.72-1494C>A ENSP00000346607.2:n.72-1494C>A
ENST00000480043.1:n.329+126C>A
NM_001202855.2:c.432+126C>A NP_001189784.1:n.432+126C>A
NM_017460.5:c.432+126C>A NP_059488.2:n.432+126C>A
XM_011515841.1:c.432+126C>A XP_011514143.1:n.432+126C>A
XM_011515842.1:c.432+126C>A XP_011514144.1:n.432+126C>A
NM_017460.6:c.432+126C>A MANE Select NP_059488.2:n.432+126C>A
NM_001202855.3:c.432+126C>A NP_001189784.1:n.432+126C>A