Canonical Allele Identifier: CA470841211

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797002A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037245A>T , CM000672.2:g.95037245A>T	GRCh38
NC_000010.10:g.96797002A>T , CM000672.1:g.96797002A>T	GRCh37
NC_000010.9:g.96786992A>T	NCBI36
NG_007972.1:g.37253T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1356T>A MANE Select	ENSP00000360317.3:p.Ile452=
ENST00000371270.5:c.1356T>A	ENSP00000360317.3:p.Ile452=
ENST00000490994.6:c.*1142T>A	ENSP00000433314.1:n.*1142T>A
ENST00000525991.5:c.*931T>A	ENSP00000433842.1:n.*931T>A
ENST00000526814.5:n.1611T>A
ENST00000527420.5:c.*213T>A	ENSP00000433191.1:n.*213T>A
ENST00000527953.5:n.1650T>A
ENST00000531714.1:n.544T>A
ENST00000533320.5:n.1590T>A
ENST00000535898.5:c.1050T>A	ENSP00000445062.1:p.Ile350=
ENST00000539050.5:c.1146T>A	ENSP00000442343.2:p.Ile382=
ENST00000623108.3:c.1146T>A	ENSP00000485110.1:p.Ile382=
NM_000770.3:c.1356T>A MANE Select	NP_000761.3:p.Ile452=
NM_001198853.1:c.1146T>A	NP_001185782.1:p.Ile382=
NM_001198854.1:c.1050T>A	NP_001185783.1:p.Ile350=
NM_001198855.1:c.1146T>A	NP_001185784.1:p.Ile382=
XR_945610.1:n.1491T>A