Canonical Allele Identifier: CA653612267

Gene: CYP2C8

Linked Data

• COSMIC: COSN21583312 ; COSN24070345

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037112_95037113insC , CM000672.2:g.95037112_95037113insC	GRCh38
NC_000010.10:g.96796869_96796870insC , CM000672.1:g.96796869_96796870insC	GRCh37
NC_000010.9:g.96786859_96786860insC	NCBI36
NG_007972.1:g.37385_37386insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*15_*16insG MANE Select	ENSP00000360317.3:n.*15_*16insG
ENST00000371270.5:c.*15_*16insG	ENSP00000360317.3:n.*15_*16insG
ENST00000490994.6:c.*1274_*1275insG	ENSP00000433314.1:n.*1274_*1275insG
ENST00000525991.5:c.*1063_*1064insG	ENSP00000433842.1:n.*1063_*1064insG
ENST00000526814.5:n.1743_1744insG
ENST00000527420.5:c.*345_*346insG	ENSP00000433191.1:n.*345_*346insG
ENST00000527953.5:n.1782_1783insG
ENST00000533320.5:n.1722_1723insG
ENST00000535898.5:c.*15_*16insG	ENSP00000445062.1:n.*15_*16insG
ENST00000539050.5:c.*15_*16insG	ENSP00000442343.2:n.*15_*16insG
ENST00000623108.3:c.*15_*16insG	ENSP00000485110.1:n.*15_*16insG
NM_000770.3:c.*15_*16insG MANE Select	NP_000761.3:n.*15_*16insG
NM_001198853.1:c.*15_*16insG	NP_001185782.1:n.*15_*16insG
NM_001198854.1:c.*15_*16insG	NP_001185783.1:n.*15_*16insG
NM_001198855.1:c.*15_*16insG	NP_001185784.1:n.*15_*16insG