Canonical Allele Identifier: CA377677587

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797057A>C (hg19) ; chr10:g.95037300A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037300A>C , CM000672.2:g.95037300A>C	GRCh38
NC_000010.10:g.96797057A>C , CM000672.1:g.96797057A>C	GRCh37
NC_000010.9:g.96787047A>C	NCBI36
NG_007972.1:g.37198T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1301T>G MANE Select	ENSP00000360317.3:p.Ile434Ser
ENST00000371270.5:c.1301T>G	ENSP00000360317.3:p.Ile434Ser
ENST00000490994.6:c.*1087T>G	ENSP00000433314.1:n.*1087T>G
ENST00000525991.5:c.*876T>G	ENSP00000433842.1:n.*876T>G
ENST00000526814.5:n.1556T>G
ENST00000527420.5:c.*158T>G	ENSP00000433191.1:n.*158T>G
ENST00000527953.5:n.1595T>G
ENST00000531714.1:n.489T>G
ENST00000533320.5:n.1535T>G
ENST00000535898.5:c.995T>G	ENSP00000445062.1:p.Ile332Ser
ENST00000539050.5:c.1091T>G	ENSP00000442343.2:p.Ile364Ser
ENST00000623108.3:c.1091T>G	ENSP00000485110.1:p.Ile364Ser
NM_000770.3:c.1301T>G MANE Select	NP_000761.3:p.Ile434Ser
NM_001198853.1:c.1091T>G	NP_001185782.1:p.Ile364Ser
NM_001198854.1:c.995T>G	NP_001185783.1:p.Ile332Ser
NM_001198855.1:c.1091T>G	NP_001185784.1:p.Ile364Ser
XR_945610.1:n.1436T>G