Canonical Allele Identifier: CA368368682

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1310881289
• gnomAD v2: 7-99358563-T-A
• MyVariant Identifiers: chr7:g.99358563T>A (hg19) ; chr7:g.99760940T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760940T>A , CM000669.2:g.99760940T>A	GRCh38
NC_000007.13:g.99358563T>A , CM000669.1:g.99358563T>A	GRCh37
NC_000007.12:g.99196499T>A	NCBI36
NG_008421.1:g.28246A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1388A>T	ENSP00000337915.3:p.Tyr463Phe
ENST00000651162.1:n.730A>T
ENST00000651514.1:c.1295A>T MANE Select	ENSP00000498939.1:p.Tyr432Phe
ENST00000651783.1:c.836A>T	ENSP00000498924.1:p.Tyr279Phe
ENST00000652018.1:c.1148A>T	ENSP00000498733.1:p.Tyr383Phe
ENST00000336411.6:c.1295A>T	ENSP00000337915.2:p.Tyr432Phe
ENST00000354593.6:c.845A>T	ENSP00000346607.2:p.Tyr282Phe
NM_001202855.2:c.1292A>T	NP_001189784.1:p.Tyr431Phe
NM_017460.5:c.1295A>T	NP_059488.2:p.Tyr432Phe
XM_011515841.1:c.1388A>T	XP_011514143.1:p.Tyr463Phe
XM_011515842.1:c.1385A>T	XP_011514144.1:p.Tyr462Phe
NM_017460.6:c.1295A>T MANE Select	NP_059488.2:p.Tyr432Phe
NM_001202855.3:c.1292A>T	NP_001189784.1:p.Tyr431Phe