Canonical Allele Identifier: CA470841267

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96798664A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038907A>C , CM000672.2:g.95038907A>C	GRCh38
NC_000010.10:g.96798664A>C , CM000672.1:g.96798664A>C	GRCh37
NC_000010.9:g.96788654A>C	NCBI36
NG_007972.1:g.35591T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1281T>G MANE Select	ENSP00000360317.3:p.Pro427=
ENST00000371270.5:c.1281T>G	ENSP00000360317.3:p.Pro427=
ENST00000490994.6:c.*1067T>G	ENSP00000433314.1:n.*1067T>G
ENST00000525991.5:c.*856T>G	ENSP00000433842.1:n.*856T>G
ENST00000526814.5:n.1536T>G
ENST00000527420.5:c.*138T>G	ENSP00000433191.1:n.*138T>G
ENST00000527953.5:n.1575T>G
ENST00000531714.1:n.469T>G
ENST00000533320.5:n.1515T>G
ENST00000535898.5:c.975T>G	ENSP00000445062.1:p.Pro325=
ENST00000539050.5:c.1071T>G	ENSP00000442343.2:p.Pro357=
ENST00000623108.3:c.1071T>G	ENSP00000485110.1:p.Pro357=
NM_000770.3:c.1281T>G MANE Select	NP_000761.3:p.Pro427=
NM_001198853.1:c.1071T>G	NP_001185782.1:p.Pro357=
NM_001198854.1:c.975T>G	NP_001185783.1:p.Pro325=
NM_001198855.1:c.1071T>G	NP_001185784.1:p.Pro357=
XR_945610.1:n.1416T>G