Canonical Allele Identifier: CA456689903

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99364856A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767233A>G , CM000669.2:g.99767233A>G	GRCh38
NC_000007.13:g.99364856A>G , CM000669.1:g.99364856A>G	GRCh37
NC_000007.12:g.99202792A>G	NCBI36
NG_008421.1:g.21953T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.696T>C	ENSP00000337915.3:p.Ile232=
ENST00000651162.1:n.131T>C
ENST00000651514.1:c.696T>C MANE Select	ENSP00000498939.1:p.Ile232=
ENST00000651783.1:c.237T>C	ENSP00000498924.1:p.Ile79=
ENST00000652018.1:c.549T>C	ENSP00000498733.1:p.Ile183=
ENST00000336411.6:c.696T>C	ENSP00000337915.2:p.Ile232=
ENST00000354593.6:c.246T>C	ENSP00000346607.2:p.Ile82=
NM_001202855.2:c.693T>C	NP_001189784.1:p.Ile231=
NM_017460.5:c.696T>C	NP_059488.2:p.Ile232=
XM_011515841.1:c.696T>C	XP_011514143.1:p.Ile232=
XM_011515842.1:c.693T>C	XP_011514144.1:p.Ile231=
NM_017460.6:c.696T>C MANE Select	NP_059488.2:p.Ile232=
NM_001202855.3:c.693T>C	NP_001189784.1:p.Ile231=