Canonical Allele Identifier: CA163151141

Gene: CYP3A4

Linked Data

• dbSNP Id: rs567089575
• gnomAD v3: 7-99760914-T-C
• gnomAD v4: 7-99760914-T-C
• MyVariant Identifiers: chr7:g.99358537T>C (hg19) ; chr7:g.99760914T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760914T>C , CM000669.2:g.99760914T>C	GRCh38
NC_000007.13:g.99358537T>C , CM000669.1:g.99358537T>C	GRCh37
NC_000007.12:g.99196473T>C	NCBI36
NG_008421.1:g.28272A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1414A>G	ENSP00000337915.3:p.Asn472Asp
ENST00000651162.1:n.756A>G
ENST00000651514.1:c.1321A>G MANE Select	ENSP00000498939.1:p.Asn441Asp
ENST00000651783.1:c.862A>G	ENSP00000498924.1:p.Asn288Asp
ENST00000652018.1:c.1174A>G	ENSP00000498733.1:p.Asn392Asp
ENST00000336411.6:c.1321A>G	ENSP00000337915.2:p.Asn441Asp
ENST00000354593.6:c.871A>G	ENSP00000346607.2:p.Asn291Asp
NM_001202855.2:c.1318A>G	NP_001189784.1:p.Asn440Asp
NM_017460.5:c.1321A>G	NP_059488.2:p.Asn441Asp
XM_011515841.1:c.1414A>G	XP_011514143.1:p.Asn472Asp
XM_011515842.1:c.1411A>G	XP_011514144.1:p.Asn471Asp
NM_017460.6:c.1321A>G MANE Select	NP_059488.2:p.Asn441Asp
NM_001202855.3:c.1318A>G	NP_001189784.1:p.Asn440Asp