Canonical Allele Identifier: CA1929375595

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037368_95037369delinsAC , CM000672.2:g.95037368_95037369delinsAC	GRCh38
NC_000010.10:g.96797125_96797126delinsAC , CM000672.1:g.96797125_96797126delinsAC	GRCh37
NC_000010.9:g.96787115_96787116delinsAC	NCBI36
NG_007972.1:g.37129_37130delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-60_1292-59delinsGT MANE Select	ENSP00000360317.3:n.1292-60_1292-59delinsGT
ENST00000371270.5:c.1292-60_1292-59delinsGT	ENSP00000360317.3:n.1292-60_1292-59delinsGT
ENST00000490994.6:c.*1078-60_*1078-59delinsGT	ENSP00000433314.1:n.*1078-60_*1078-59delinsGT
ENST00000525991.5:c.*867-60_*867-59delinsGT	ENSP00000433842.1:n.*867-60_*867-59delinsGT
ENST00000526814.5:n.1547-60_1547-59delinsGT
ENST00000527420.5:c.*149-60_*149-59delinsGT	ENSP00000433191.1:n.*149-60_*149-59delinsGT
ENST00000527953.5:n.1586-60_1586-59delinsGT
ENST00000531714.1:n.480-60_480-59delinsGT
ENST00000533320.5:n.1526-60_1526-59delinsGT
ENST00000535898.5:c.986-60_986-59delinsGT	ENSP00000445062.1:n.986-60_986-59delinsGT
ENST00000539050.5:c.1082-60_1082-59delinsGT	ENSP00000442343.2:n.1082-60_1082-59delinsGT
ENST00000623108.3:c.1082-60_1082-59delinsGT	ENSP00000485110.1:n.1082-60_1082-59delinsGT
NM_000770.3:c.1292-60_1292-59delinsGT MANE Select	NP_000761.3:n.1292-60_1292-59delinsGT
NM_001198853.1:c.1082-60_1082-59delinsGT	NP_001185782.1:n.1082-60_1082-59delinsGT
NM_001198854.1:c.986-60_986-59delinsGT	NP_001185783.1:n.986-60_986-59delinsGT
NM_001198855.1:c.1082-60_1082-59delinsGT	NP_001185784.1:n.1082-60_1082-59delinsGT
XR_945610.1:n.1427-60_1427-59delinsGT