Canonical Allele Identifier: CA368369289

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99359796T>A (hg19) ; chr7:g.99762173T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762173T>A , CM000669.2:g.99762173T>A	GRCh38
NC_000007.13:g.99359796T>A , CM000669.1:g.99359796T>A	GRCh37
NC_000007.12:g.99197732T>A	NCBI36
NG_008421.1:g.27013A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1121A>T	ENSP00000337915.3:p.Glu374Val
ENST00000651162.1:n.556A>T
ENST00000651514.1:c.1121A>T MANE Select	ENSP00000498939.1:p.Glu374Val
ENST00000651783.1:c.662A>T	ENSP00000498924.1:p.Glu221Val
ENST00000652018.1:c.974A>T	ENSP00000498733.1:p.Glu325Val
ENST00000336411.6:c.1121A>T	ENSP00000337915.2:p.Glu374Val
ENST00000354593.6:c.671A>T	ENSP00000346607.2:p.Glu224Val
NM_001202855.2:c.1118A>T	NP_001189784.1:p.Glu373Val
NM_017460.5:c.1121A>T	NP_059488.2:p.Glu374Val
XM_011515841.1:c.1121A>T	XP_011514143.1:p.Glu374Val
XM_011515842.1:c.1118A>T	XP_011514144.1:p.Glu373Val
NM_017460.6:c.1121A>T MANE Select	NP_059488.2:p.Glu374Val
NM_001202855.3:c.1118A>T	NP_001189784.1:p.Glu373Val