Canonical Allele Identifier: CA163151158
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs1041988

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99760943A>G , CM000669.2:g.99760943A>G GRCh38
NC_000007.13:g.99358566A>G , CM000669.1:g.99358566A>G GRCh37
NC_000007.12:g.99196502A>G NCBI36
NG_008421.1:g.28243T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.1385T>C ENSP00000337915.3:p.Ile462Thr
ENST00000651162.1:n.727T>C
ENST00000651514.1:c.1292T>C MANE Select ENSP00000498939.1:p.Ile431Thr
ENST00000651783.1:c.833T>C ENSP00000498924.1:p.Ile278Thr
ENST00000652018.1:c.1145T>C ENSP00000498733.1:p.Ile382Thr
ENST00000336411.6:c.1292T>C ENSP00000337915.2:p.Ile431Thr
ENST00000354593.6:c.842T>C ENSP00000346607.2:p.Ile281Thr
NM_001202855.2:c.1289T>C NP_001189784.1:p.Ile430Thr
NM_017460.5:c.1292T>C NP_059488.2:p.Ile431Thr
XM_011515841.1:c.1385T>C XP_011514143.1:p.Ile462Thr
XM_011515842.1:c.1382T>C XP_011514144.1:p.Ile461Thr
NM_017460.6:c.1292T>C MANE Select NP_059488.2:p.Ile431Thr
NM_001202855.3:c.1289T>C NP_001189784.1:p.Ile430Thr