Canonical Allele Identifier: CA368369022
Gene: CYP3A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99762116A>G , CM000669.2:g.99762116A>G GRCh38
NC_000007.13:g.99359739A>G , CM000669.1:g.99359739A>G GRCh37
NC_000007.12:g.99197675A>G NCBI36
NG_008421.1:g.27070T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.1178T>C ENSP00000337915.3:p.Val393Ala
ENST00000651162.1:n.613T>C
ENST00000651514.1:c.1178T>C MANE Select ENSP00000498939.1:p.Val393Ala
ENST00000651783.1:c.719T>C ENSP00000498924.1:p.Val240Ala
ENST00000652018.1:c.1031T>C ENSP00000498733.1:p.Val344Ala
ENST00000336411.6:c.1178T>C ENSP00000337915.2:p.Val393Ala
ENST00000354593.6:c.728T>C ENSP00000346607.2:p.Val243Ala
NM_001202855.2:c.1175T>C NP_001189784.1:p.Val392Ala
NM_017460.5:c.1178T>C NP_059488.2:p.Val393Ala
XM_011515841.1:c.1178T>C XP_011514143.1:p.Val393Ala
XM_011515842.1:c.1175T>C XP_011514144.1:p.Val392Ala
NM_017460.6:c.1178T>C MANE Select NP_059488.2:p.Val393Ala
NM_001202855.3:c.1175T>C NP_001189784.1:p.Val392Ala