Canonical Allele Identifier: CA2574620341

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037360_95037365del , CM000672.2:g.95037360_95037365del	GRCh38
NC_000010.10:g.96797117_96797122del , CM000672.1:g.96797117_96797122del	GRCh37
NC_000010.9:g.96787107_96787112del	NCBI36
NG_007972.1:g.37141_37146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-48_1292-43del MANE Select	ENSP00000360317.3:n.1292-48_1292-43del
ENST00000371270.5:c.1292-48_1292-43del	ENSP00000360317.3:n.1292-48_1292-43del
ENST00000490994.6:c.*1078-48_*1078-43del	ENSP00000433314.1:n.*1078-48_*1078-43del
ENST00000525991.5:c.*867-48_*867-43del	ENSP00000433842.1:n.*867-48_*867-43del
ENST00000526814.5:n.1547-48_1547-43del
ENST00000527420.5:c.*149-48_*149-43del	ENSP00000433191.1:n.*149-48_*149-43del
ENST00000527953.5:n.1586-48_1586-43del
ENST00000531714.1:n.480-48_480-43del
ENST00000533320.5:n.1526-48_1526-43del
ENST00000535898.5:c.986-48_986-43del	ENSP00000445062.1:n.986-48_986-43del
ENST00000539050.5:c.1082-48_1082-43del	ENSP00000442343.2:n.1082-48_1082-43del
ENST00000623108.3:c.1082-48_1082-43del	ENSP00000485110.1:n.1082-48_1082-43del
NM_000770.3:c.1292-48_1292-43del MANE Select	NP_000761.3:n.1292-48_1292-43del
NM_001198853.1:c.1082-48_1082-43del	NP_001185782.1:n.1082-48_1082-43del
NM_001198854.1:c.986-48_986-43del	NP_001185783.1:n.986-48_986-43del
NM_001198855.1:c.1082-48_1082-43del	NP_001185784.1:n.1082-48_1082-43del
XR_945610.1:n.1427-48_1427-43del