Canonical Allele Identifier: CA368370003

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1214066754
• gnomAD v2: 7-99364011-T-C
• gnomAD v3: 7-99766388-T-C
• gnomAD v4: 7-99766388-T-C
• MyVariant Identifiers: chr7:g.99364011T>C (hg19) ; chr7:g.99766388T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99766388T>C , CM000669.2:g.99766388T>C	GRCh38
NC_000007.13:g.99364011T>C , CM000669.1:g.99364011T>C	GRCh37
NC_000007.12:g.99201947T>C	NCBI36
NG_008421.1:g.22798A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.854A>G	ENSP00000337915.3:p.Glu285Gly
ENST00000651162.1:n.289A>G
ENST00000651514.1:c.854A>G MANE Select	ENSP00000498939.1:p.Glu285Gly
ENST00000651783.1:c.395A>G	ENSP00000498924.1:p.Glu132Gly
ENST00000652018.1:c.707A>G	ENSP00000498733.1:p.Glu236Gly
ENST00000336411.6:c.854A>G	ENSP00000337915.2:p.Glu285Gly
ENST00000354593.6:c.404A>G	ENSP00000346607.2:p.Glu135Gly
NM_001202855.2:c.851A>G	NP_001189784.1:p.Glu284Gly
NM_017460.5:c.854A>G	NP_059488.2:p.Glu285Gly
XM_011515841.1:c.854A>G	XP_011514143.1:p.Glu285Gly
XM_011515842.1:c.851A>G	XP_011514144.1:p.Glu284Gly
NM_017460.6:c.854A>G MANE Select	NP_059488.2:p.Glu285Gly
NM_001202855.3:c.851A>G	NP_001189784.1:p.Glu284Gly