Canonical Allele Identifier: CA4369782

Gene: CYP3A4

Linked Data

• dbSNP Id: rs748236460
• ExAC: 7:99367771 T / C
• gnomAD v2: 7-99367771-T-C
• gnomAD v3: 7-99770148-T-C
• gnomAD v4: 7-99770148-T-C
• MyVariant Identifiers: chr7:g.99367771T>C (hg19) ; chr7:g.99770148T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770148T>C , CM000669.2:g.99770148T>C	GRCh38
NC_000007.13:g.99367771T>C , CM000669.1:g.99367771T>C	GRCh37
NC_000007.12:g.99205707T>C	NCBI36
NG_008421.1:g.19038A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.406A>G	ENSP00000337915.3:p.Thr136Ala
ENST00000651514.1:c.406A>G MANE Select	ENSP00000498939.1:p.Thr136Ala
ENST00000651783.1:c.58-1641A>G	ENSP00000498924.1:n.58-1641A>G
ENST00000652018.1:c.259A>G	ENSP00000498733.1:p.Thr87Ala
ENST00000336411.6:c.406A>G	ENSP00000337915.2:p.Thr136Ala
ENST00000354593.6:c.72-1646A>G	ENSP00000346607.2:n.72-1646A>G
ENST00000415003.1:c.445A>G	ENSP00000397208.1:p.Thr149Ala
ENST00000480043.1:n.303A>G
NM_001202855.2:c.406A>G	NP_001189784.1:p.Thr136Ala
NM_017460.5:c.406A>G	NP_059488.2:p.Thr136Ala
XM_011515841.1:c.406A>G	XP_011514143.1:p.Thr136Ala
XM_011515842.1:c.406A>G	XP_011514144.1:p.Thr136Ala
NM_017460.6:c.406A>G MANE Select	NP_059488.2:p.Thr136Ala
NM_001202855.3:c.406A>G	NP_001189784.1:p.Thr136Ala