Canonical Allele Identifier: CA2578955207
Gene: CYP3A4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769678A>G , CM000669.2:g.99769678A>G GRCh38
NC_000007.13:g.99367301A>G , CM000669.1:g.99367301A>G GRCh37
NC_000007.12:g.99205237A>G NCBI36
NG_008421.1:g.19508T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.521+90T>C ENSP00000337915.3:n.521+90T>C
ENST00000651514.1:c.521+90T>C MANE Select ENSP00000498939.1:n.521+90T>C
ENST00000651783.1:c.58-1171T>C ENSP00000498924.1:n.58-1171T>C
ENST00000652018.1:c.374+90T>C ENSP00000498733.1:n.374+90T>C
ENST00000336411.6:c.521+90T>C ENSP00000337915.2:n.521+90T>C
ENST00000354593.6:c.72-1176T>C ENSP00000346607.2:n.72-1176T>C
ENST00000480043.1:n.508T>C
NM_001202855.2:c.521+90T>C NP_001189784.1:n.521+90T>C
NM_017460.5:c.521+90T>C NP_059488.2:n.521+90T>C
XM_011515841.1:c.521+90T>C XP_011514143.1:n.521+90T>C
XM_011515842.1:c.521+90T>C XP_011514144.1:n.521+90T>C
NM_017460.6:c.521+90T>C MANE Select NP_059488.2:n.521+90T>C
NM_001202855.3:c.521+90T>C NP_001189784.1:n.521+90T>C
Search 100 bp 5'
Search 100 bp 3'