Canonical Allele Identifier: CA456689779

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99364814T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767191T>C , CM000669.2:g.99767191T>C	GRCh38
NC_000007.13:g.99364814T>C , CM000669.1:g.99364814T>C	GRCh37
NC_000007.12:g.99202750T>C	NCBI36
NG_008421.1:g.21995A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.738A>G	ENSP00000337915.3:p.Thr246=
ENST00000651162.1:n.173A>G
ENST00000651514.1:c.738A>G MANE Select	ENSP00000498939.1:p.Thr246=
ENST00000651783.1:c.279A>G	ENSP00000498924.1:p.Thr93=
ENST00000652018.1:c.591A>G	ENSP00000498733.1:p.Thr197=
ENST00000336411.6:c.738A>G	ENSP00000337915.2:p.Thr246=
ENST00000354593.6:c.288A>G	ENSP00000346607.2:p.Thr96=
NM_001202855.2:c.735A>G	NP_001189784.1:p.Thr245=
NM_017460.5:c.738A>G	NP_059488.2:p.Thr246=
XM_011515841.1:c.738A>G	XP_011514143.1:p.Thr246=
XM_011515842.1:c.735A>G	XP_011514144.1:p.Thr245=
NM_017460.6:c.738A>G MANE Select	NP_059488.2:p.Thr246=
NM_001202855.3:c.735A>G	NP_001189784.1:p.Thr245=