Canonical Allele Identifier: CA368371134

Gene: CYP3A4

Linked Data

• dbSNP Id: rs139541290
• gnomAD v2: 7-99366075-A-T
• gnomAD v4: 7-99768452-A-T
• MyVariant Identifiers: chr7:g.99366075A>T (hg19) ; chr7:g.99768452A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768452A>T , CM000669.2:g.99768452A>T	GRCh38
NC_000007.13:g.99366075A>T , CM000669.1:g.99366075A>T	GRCh37
NC_000007.12:g.99204011A>T	NCBI36
NG_008421.1:g.20734T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.572T>A	ENSP00000337915.3:p.Val191Glu
ENST00000651514.1:c.572T>A MANE Select	ENSP00000498939.1:p.Val191Glu
ENST00000651783.1:c.113T>A	ENSP00000498924.1:p.Val38Glu
ENST00000652018.1:c.425T>A	ENSP00000498733.1:p.Val142Glu
ENST00000336411.6:c.572T>A	ENSP00000337915.2:p.Val191Glu
ENST00000354593.6:c.122T>A	ENSP00000346607.2:p.Val41Glu
NM_001202855.2:c.572T>A	NP_001189784.1:p.Val191Glu
NM_017460.5:c.572T>A	NP_059488.2:p.Val191Glu
XM_011515841.1:c.572T>A	XP_011514143.1:p.Val191Glu
XM_011515842.1:c.572T>A	XP_011514144.1:p.Val191Glu
NM_017460.6:c.572T>A MANE Select	NP_059488.2:p.Val191Glu
NM_001202855.3:c.572T>A	NP_001189784.1:p.Val191Glu