Canonical Allele Identifier: CA2789074447

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037726_95037729del , CM000672.2:g.95037726_95037729del	GRCh38
NC_000010.10:g.96797483_96797486del , CM000672.1:g.96797483_96797486del	GRCh37
NC_000010.9:g.96787473_96787476del	NCBI36
NG_007972.1:g.36769_36772del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1292-420_1292-417del MANE Select	ENSP00000360317.3:n.1292-420_1292-417del
ENST00000371270.5:c.1292-420_1292-417del	ENSP00000360317.3:n.1292-420_1292-417del
ENST00000490994.6:c.*1078-420_*1078-417del	ENSP00000433314.1:n.*1078-420_*1078-417del
ENST00000525991.5:c.*867-420_*867-417del	ENSP00000433842.1:n.*867-420_*867-417del
ENST00000526814.5:n.1547-420_1547-417del
ENST00000527420.5:c.*149-420_*149-417del	ENSP00000433191.1:n.*149-420_*149-417del
ENST00000527953.5:n.1586-420_1586-417del
ENST00000531714.1:n.480-420_480-417del
ENST00000533320.5:n.1526-420_1526-417del
ENST00000535898.5:c.986-420_986-417del	ENSP00000445062.1:n.986-420_986-417del
ENST00000539050.5:c.1082-420_1082-417del	ENSP00000442343.2:n.1082-420_1082-417del
ENST00000623108.3:c.1082-420_1082-417del	ENSP00000485110.1:n.1082-420_1082-417del
NM_000770.3:c.1292-420_1292-417del MANE Select	NP_000761.3:n.1292-420_1292-417del
NM_001198853.1:c.1082-420_1082-417del	NP_001185782.1:n.1082-420_1082-417del
NM_001198854.1:c.986-420_986-417del	NP_001185783.1:n.986-420_986-417del
NM_001198855.1:c.1082-420_1082-417del	NP_001185784.1:n.1082-420_1082-417del
XR_945610.1:n.1427-420_1427-417del