Canonical Allele Identifier: CA470841222

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797020A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037263A>G , CM000672.2:g.95037263A>G	GRCh38
NC_000010.10:g.96797020A>G , CM000672.1:g.96797020A>G	GRCh37
NC_000010.9:g.96787010A>G	NCBI36
NG_007972.1:g.37235T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1338T>C MANE Select	ENSP00000360317.3:p.Phe446=
ENST00000371270.5:c.1338T>C	ENSP00000360317.3:p.Phe446=
ENST00000490994.6:c.*1124T>C	ENSP00000433314.1:n.*1124T>C
ENST00000525991.5:c.*913T>C	ENSP00000433842.1:n.*913T>C
ENST00000526814.5:n.1593T>C
ENST00000527420.5:c.*195T>C	ENSP00000433191.1:n.*195T>C
ENST00000527953.5:n.1632T>C
ENST00000531714.1:n.526T>C
ENST00000533320.5:n.1572T>C
ENST00000535898.5:c.1032T>C	ENSP00000445062.1:p.Phe344=
ENST00000539050.5:c.1128T>C	ENSP00000442343.2:p.Phe376=
ENST00000623108.3:c.1128T>C	ENSP00000485110.1:p.Phe376=
NM_000770.3:c.1338T>C MANE Select	NP_000761.3:p.Phe446=
NM_001198853.1:c.1128T>C	NP_001185782.1:p.Phe376=
NM_001198854.1:c.1032T>C	NP_001185783.1:p.Phe344=
NM_001198855.1:c.1128T>C	NP_001185784.1:p.Phe376=
XR_945610.1:n.1473T>C