Canonical Allele Identifier: CA377677397

Gene: CYP2C8

Linked Data

• COSMIC: COSM3415386 ; COSM3415387
• MyVariant Identifiers: chr10:g.96796968A>C (hg19) ; chr10:g.95037211A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037211A>C , CM000672.2:g.95037211A>C	GRCh38
NC_000010.10:g.96796968A>C , CM000672.1:g.96796968A>C	GRCh37
NC_000010.9:g.96786958A>C	NCBI36
NG_007972.1:g.37287T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1390T>G MANE Select	ENSP00000360317.3:p.Leu464Val
ENST00000371270.5:c.1390T>G	ENSP00000360317.3:p.Leu464Val
ENST00000490994.6:c.*1176T>G	ENSP00000433314.1:n.*1176T>G
ENST00000525991.5:c.*965T>G	ENSP00000433842.1:n.*965T>G
ENST00000526814.5:n.1645T>G
ENST00000527420.5:c.*247T>G	ENSP00000433191.1:n.*247T>G
ENST00000527953.5:n.1684T>G
ENST00000531714.1:n.578T>G
ENST00000533320.5:n.1624T>G
ENST00000535898.5:c.1084T>G	ENSP00000445062.1:p.Leu362Val
ENST00000539050.5:c.1180T>G	ENSP00000442343.2:p.Leu394Val
ENST00000623108.3:c.1180T>G	ENSP00000485110.1:p.Leu394Val
NM_000770.3:c.1390T>G MANE Select	NP_000761.3:p.Leu464Val
NM_001198853.1:c.1180T>G	NP_001185782.1:p.Leu394Val
NM_001198854.1:c.1084T>G	NP_001185783.1:p.Leu362Val
NM_001198855.1:c.1180T>G	NP_001185784.1:p.Leu394Val
XR_945610.1:n.1525T>G