Canonical Allele Identifier: CA163151106

Gene: CYP3A4

Linked Data

• dbSNP Id: rs71583803
• gnomAD v3: 7-99760847-A-C
• gnomAD v4: 7-99760847-A-C
• MyVariant Identifiers: chr7:g.99358470A>C (hg19) ; chr7:g.99760847A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760847A>C , CM000669.2:g.99760847A>C	GRCh38
NC_000007.13:g.99358470A>C , CM000669.1:g.99358470A>C	GRCh37
NC_000007.12:g.99196406A>C	NCBI36
NG_008421.1:g.28339T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1481T>G	ENSP00000337915.3:p.Phe494Cys
ENST00000651162.1:n.823T>G
ENST00000651514.1:c.1388T>G MANE Select	ENSP00000498939.1:p.Phe463Cys
ENST00000651783.1:c.929T>G	ENSP00000498924.1:p.Phe310Cys
ENST00000652018.1:c.1241T>G	ENSP00000498733.1:p.Phe414Cys
ENST00000336411.6:c.1388T>G	ENSP00000337915.2:p.Phe463Cys
ENST00000354593.6:c.938T>G	ENSP00000346607.2:p.Phe313Cys
NM_001202855.2:c.1385T>G	NP_001189784.1:p.Phe462Cys
NM_017460.5:c.1388T>G	NP_059488.2:p.Phe463Cys
XM_011515841.1:c.1481T>G	XP_011514143.1:p.Phe494Cys
XM_011515842.1:c.1478T>G	XP_011514144.1:p.Phe493Cys
NM_017460.6:c.1388T>G MANE Select	NP_059488.2:p.Phe463Cys
NM_001202855.3:c.1385T>G	NP_001189784.1:p.Phe462Cys