Canonical Allele Identifier: CA377682835

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827012A>G (hg19) ; chr10:g.95067255A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067255A>G , CM000672.2:g.95067255A>G	GRCh38
NC_000010.10:g.96827012A>G , CM000672.1:g.96827012A>G	GRCh37
NC_000010.9:g.96817002A>G	NCBI36
NG_007972.1:g.7243T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.434T>C MANE Select	ENSP00000360317.3:p.Val145Ala
ENST00000371270.5:c.434T>C	ENSP00000360317.3:p.Val145Ala
ENST00000479946.2:n.738T>C
ENST00000490994.6:c.*220T>C	ENSP00000433314.1:n.*220T>C
ENST00000525991.5:c.*9T>C	ENSP00000433842.1:n.*9T>C
ENST00000526814.5:n.689T>C
ENST00000527420.5:c.434T>C	ENSP00000433191.1:p.Val145Ala
ENST00000527953.5:n.689T>C
ENST00000533320.5:n.668T>C
ENST00000535898.5:c.128T>C	ENSP00000445062.1:p.Val43Ala
ENST00000539050.5:c.224T>C	ENSP00000442343.2:p.Val75Ala
ENST00000623108.3:c.224T>C	ENSP00000485110.1:p.Val75Ala
ENST00000628935.1:c.176T>C	ENSP00000487145.1:p.Val59Ala
NM_000770.3:c.434T>C MANE Select	NP_000761.3:p.Val145Ala
NM_001198853.1:c.224T>C	NP_001185782.1:p.Val75Ala
NM_001198854.1:c.128T>C	NP_001185783.1:p.Val43Ala
NM_001198855.1:c.224T>C	NP_001185784.1:p.Val75Ala
XR_945610.1:n.530T>C