Canonical Allele Identifier: CA470841145

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796912T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037155T>G , CM000672.2:g.95037155T>G	GRCh38
NC_000010.10:g.96796912T>G , CM000672.1:g.96796912T>G	GRCh37
NC_000010.9:g.96786902T>G	NCBI36
NG_007972.1:g.37343A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1446A>C MANE Select	ENSP00000360317.3:p.Ser482=
ENST00000371270.5:c.1446A>C	ENSP00000360317.3:p.Ser482=
ENST00000490994.6:c.*1232A>C	ENSP00000433314.1:n.*1232A>C
ENST00000525991.5:c.*1021A>C	ENSP00000433842.1:n.*1021A>C
ENST00000526814.5:n.1701A>C
ENST00000527420.5:c.*303A>C	ENSP00000433191.1:n.*303A>C
ENST00000527953.5:n.1740A>C
ENST00000533320.5:n.1680A>C
ENST00000535898.5:c.1140A>C	ENSP00000445062.1:p.Ser380=
ENST00000539050.5:c.1236A>C	ENSP00000442343.2:p.Ser412=
ENST00000623108.3:c.1236A>C	ENSP00000485110.1:p.Ser412=
NM_000770.3:c.1446A>C MANE Select	NP_000761.3:p.Ser482=
NM_001198853.1:c.1236A>C	NP_001185782.1:p.Ser412=
NM_001198854.1:c.1140A>C	NP_001185783.1:p.Ser380=
NM_001198855.1:c.1236A>C	NP_001185784.1:p.Ser412=