Canonical Allele Identifier: CA1929375015

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037087_95037088delinsGC , CM000672.2:g.95037087_95037088delinsGC	GRCh38
NC_000010.10:g.96796844_96796845delinsGC , CM000672.1:g.96796844_96796845delinsGC	GRCh37
NC_000010.9:g.96786834_96786835delinsGC	NCBI36
NG_007972.1:g.37410_37411delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*40_*41delinsGC MANE Select	ENSP00000360317.3:n.*40_*41delinsGC
ENST00000371270.5:c.*40_*41delinsGC	ENSP00000360317.3:n.*40_*41delinsGC
ENST00000490994.6:c.*1299_*1300delinsGC	ENSP00000433314.1:n.*1299_*1300delinsGC
ENST00000525991.5:c.*1088_*1089delinsGC	ENSP00000433842.1:n.*1088_*1089delinsGC
ENST00000526814.5:n.1768_1769delinsGC
ENST00000527420.5:c.*370_*371delinsGC	ENSP00000433191.1:n.*370_*371delinsGC
ENST00000527953.5:n.1807_1808delinsGC
ENST00000533320.5:n.1747_1748delinsGC
ENST00000535898.5:c.*40_*41delinsGC	ENSP00000445062.1:n.*40_*41delinsGC
ENST00000539050.5:c.*40_*41delinsGC	ENSP00000442343.2:n.*40_*41delinsGC
ENST00000623108.3:c.*40_*41delinsGC	ENSP00000485110.1:n.*40_*41delinsGC
NM_000770.3:c.*40_*41delinsGC MANE Select	NP_000761.3:n.*40_*41delinsGC
NM_001198853.1:c.*40_*41delinsGC	NP_001185782.1:n.*40_*41delinsGC
NM_001198854.1:c.*40_*41delinsGC	NP_001185783.1:n.*40_*41delinsGC
NM_001198855.1:c.*40_*41delinsGC	NP_001185784.1:n.*40_*41delinsGC