Canonical Allele Identifier: CA4369783
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs376124415
gnomAD v2: 7-99367776-G-C
gnomAD v3: 7-99770153-G-C
gnomAD v4: 7-99770153-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99770153G>C , CM000669.2:g.99770153G>C GRCh38
NC_000007.13:g.99367776G>C , CM000669.1:g.99367776G>C GRCh37
NC_000007.12:g.99205712G>C NCBI36
NG_008421.1:g.19033C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.401C>G ENSP00000337915.3:p.Ser134Cys
ENST00000651514.1:c.401C>G MANE Select ENSP00000498939.1:p.Ser134Cys
ENST00000651783.1:c.58-1646C>G ENSP00000498924.1:n.58-1646C>G
ENST00000652018.1:c.254C>G ENSP00000498733.1:p.Ser85Cys
ENST00000336411.6:c.401C>G ENSP00000337915.2:p.Ser134Cys
ENST00000354593.6:c.72-1651C>G ENSP00000346607.2:n.72-1651C>G
ENST00000415003.1:c.440C>G ENSP00000397208.1:p.Ser147Cys
ENST00000480043.1:n.298C>G
NM_001202855.2:c.401C>G NP_001189784.1:p.Ser134Cys
NM_017460.5:c.401C>G NP_059488.2:p.Ser134Cys
XM_011515841.1:c.401C>G XP_011514143.1:p.Ser134Cys
XM_011515842.1:c.401C>G XP_011514144.1:p.Ser134Cys
NM_017460.6:c.401C>G MANE Select NP_059488.2:p.Ser134Cys
NM_001202855.3:c.401C>G NP_001189784.1:p.Ser134Cys