Canonical Allele Identifier: CA4369498
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs4986910

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99760901A>G , CM000669.2:g.99760901A>G GRCh38
NC_000007.13:g.99358524A>G , CM000669.1:g.99358524A>G GRCh37
NC_000007.12:g.99196460A>G NCBI36
NG_008421.1:g.28285T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.1427T>C ENSP00000337915.3:p.Met476Thr
ENST00000651162.1:n.769T>C
ENST00000651514.1:c.1334T>C MANE Select ENSP00000498939.1:p.Met445Thr
ENST00000651783.1:n.875T>C ENSP00000498924.1:p.Met292Thr
ENST00000652018.1:c.1187T>C ENSP00000498733.1:p.Met396Thr
ENST00000336411.6:c.1334T>C ENSP00000337915.2:p.Met445Thr
ENST00000354593.6:c.884T>C ENSP00000346607.2:p.Met295Thr
NM_001202855.2:c.1331T>C NP_001189784.1:p.Met444Thr
NM_017460.5:c.1334T>C NP_059488.2:p.Met445Thr
XM_011515841.1:c.1427T>C XP_011514143.1:p.Met476Thr
XM_011515842.1:c.1424T>C XP_011514144.1:p.Met475Thr
NM_017460.6:c.1334T>C MANE Select NP_059488.2:p.Met445Thr
NM_001202855.3:c.1331T>C NP_001189784.1:p.Met444Thr