Canonical Allele Identifier: CA1929388121

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067206_95067207delinsAC , CM000672.2:g.95067206_95067207delinsAC	GRCh38
NC_000010.10:g.96826963_96826964delinsAC , CM000672.1:g.96826963_96826964delinsAC	GRCh37
NC_000010.9:g.96816953_96816954delinsAC	NCBI36
NG_007972.1:g.7291_7292delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.481+1_481+2delinsGT MANE Select	ENSP00000360317.3:n.481+1_481+2delinsGT
ENST00000371270.5:c.481+1_481+2delinsGT	ENSP00000360317.3:n.481+1_481+2delinsGT
ENST00000479946.2:n.785+1_785+2delinsGT
ENST00000490994.6:c.*267+1_*267+2delinsGT	ENSP00000433314.1:n.*267+1_*267+2delinsGT
ENST00000525991.5:c.*56+1_*56+2delinsGT	ENSP00000433842.1:n.*56+1_*56+2delinsGT
ENST00000526814.5:n.736+1_736+2delinsGT
ENST00000527420.5:c.481+1_481+2delinsGT	ENSP00000433191.1:n.481+1_481+2delinsGT
ENST00000527953.5:n.736+1_736+2delinsGT
ENST00000533320.5:n.715+1_715+2delinsGT
ENST00000535898.5:c.175+1_175+2delinsGT	ENSP00000445062.1:n.175+1_175+2delinsGT
ENST00000539050.5:c.271+1_271+2delinsGT	ENSP00000442343.2:n.271+1_271+2delinsGT
ENST00000623108.3:c.271+1_271+2delinsGT	ENSP00000485110.1:n.271+1_271+2delinsGT
ENST00000628935.1:c.223+1_223+2delinsGT	ENSP00000487145.1:n.223+1_223+2delinsGT
NM_000770.3:c.481+1_481+2delinsGT MANE Select	NP_000761.3:n.481+1_481+2delinsGT
NM_001198853.1:c.271+1_271+2delinsGT	NP_001185782.1:n.271+1_271+2delinsGT
NM_001198854.1:c.175+1_175+2delinsGT	NP_001185783.1:n.175+1_175+2delinsGT
NM_001198855.1:c.271+1_271+2delinsGT	NP_001185784.1:n.271+1_271+2delinsGT
XR_945610.1:n.577+1_577+2delinsGT