Canonical Allele Identifier: CA1929366737

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95049125_95049126delinsAT , CM000672.2:g.95049125_95049126delinsAT	GRCh38
NC_000010.10:g.96808882_96808883delinsAT , CM000672.1:g.96808882_96808883delinsAT	GRCh37
NC_000010.9:g.96798872_96798873delinsAT	NCBI36
NG_007972.1:g.25372_25373delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.820-3175_820-3174delinsAT MANE Select	ENSP00000360317.3:n.820-3175_820-3174delinsAT
ENST00000371270.5:c.820-3175_820-3174delinsAT	ENSP00000360317.3:n.820-3175_820-3174delinsAT
ENST00000479946.2:n.1124-3175_1124-3174delinsAT
ENST00000490994.6:c.*606-3175_*606-3174delinsAT	ENSP00000433314.1:n.*606-3175_*606-3174delinsAT
ENST00000525991.5:c.*395-3175_*395-3174delinsAT	ENSP00000433842.1:n.*395-3175_*395-3174delinsAT
ENST00000526814.5:n.1075-3175_1075-3174delinsAT
ENST00000527420.5:c.820-3175_820-3174delinsAT	ENSP00000433191.1:n.820-3175_820-3174delinsAT
ENST00000527953.5:n.1075-3175_1075-3174delinsAT
ENST00000533320.5:n.1054-3175_1054-3174delinsAT
ENST00000535898.5:c.514-3175_514-3174delinsAT	ENSP00000445062.1:n.514-3175_514-3174delinsAT
ENST00000539050.5:c.610-3175_610-3174delinsAT	ENSP00000442343.2:n.610-3175_610-3174delinsAT
ENST00000623108.3:c.610-3175_610-3174delinsAT	ENSP00000485110.1:n.610-3175_610-3174delinsAT
ENST00000628935.1:c.562-3175_562-3174delinsAT	ENSP00000487145.1:n.562-3175_562-3174delinsAT
NM_000770.3:c.820-3175_820-3174delinsAT MANE Select	NP_000761.3:n.820-3175_820-3174delinsAT
NM_001198853.1:c.610-3175_610-3174delinsAT	NP_001185782.1:n.610-3175_610-3174delinsAT
NM_001198854.1:c.514-3175_514-3174delinsAT	NP_001185783.1:n.514-3175_514-3174delinsAT
NM_001198855.1:c.610-3175_610-3174delinsAT	NP_001185784.1:n.610-3175_610-3174delinsAT
XR_945610.1:n.916-3175_916-3174delinsAT