Canonical Allele Identifier: CA653612213

Gene: CYP2C8

Linked Data

• COSMIC: COSN20092172

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037077_95037078insG , CM000672.2:g.95037077_95037078insG	GRCh38
NC_000010.10:g.96796834_96796835insG , CM000672.1:g.96796834_96796835insG	GRCh37
NC_000010.9:g.96786824_96786825insG	NCBI36
NG_007972.1:g.37420_37421insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*50_*51insC MANE Select	ENSP00000360317.3:n.*50_*51insC
ENST00000371270.5:c.*50_*51insC	ENSP00000360317.3:n.*50_*51insC
ENST00000490994.6:c.*1309_*1310insC	ENSP00000433314.1:n.*1309_*1310insC
ENST00000525991.5:c.*1098_*1099insC	ENSP00000433842.1:n.*1098_*1099insC
ENST00000526814.5:n.1778_1779insC
ENST00000527420.5:c.*380_*381insC	ENSP00000433191.1:n.*380_*381insC
ENST00000527953.5:n.1817_1818insC
ENST00000533320.5:n.1757_1758insC
ENST00000535898.5:c.*50_*51insC	ENSP00000445062.1:n.*50_*51insC
ENST00000539050.5:c.*50_*51insC	ENSP00000442343.2:n.*50_*51insC
ENST00000623108.3:c.*50_*51insC	ENSP00000485110.1:n.*50_*51insC
NM_000770.3:c.*50_*51insC MANE Select	NP_000761.3:n.*50_*51insC
NM_001198853.1:c.*50_*51insC	NP_001185782.1:n.*50_*51insC
NM_001198854.1:c.*50_*51insC	NP_001185783.1:n.*50_*51insC
NM_001198855.1:c.*50_*51insC	NP_001185784.1:n.*50_*51insC