Canonical Allele Identifier: CA2547210139

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037602_95037603insA , CM000672.2:g.95037602_95037603insA	GRCh38
NC_000010.10:g.96797359_96797360insA , CM000672.1:g.96797359_96797360insA	GRCh37
NC_000010.9:g.96787349_96787350insA	NCBI36
NG_007972.1:g.36895_36896insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-294_1292-293insT MANE Select	ENSP00000360317.3:n.1292-294_1292-293insT
ENST00000371270.5:c.1292-294_1292-293insT	ENSP00000360317.3:n.1292-294_1292-293insT
ENST00000490994.6:c.*1078-294_*1078-293insT	ENSP00000433314.1:n.*1078-294_*1078-293insT
ENST00000525991.5:c.*867-294_*867-293insT	ENSP00000433842.1:n.*867-294_*867-293insT
ENST00000526814.5:n.1547-294_1547-293insT
ENST00000527420.5:c.*149-294_*149-293insT	ENSP00000433191.1:n.*149-294_*149-293insT
ENST00000527953.5:n.1586-294_1586-293insT
ENST00000531714.1:n.480-294_480-293insT
ENST00000533320.5:n.1526-294_1526-293insT
ENST00000535898.5:c.986-294_986-293insT	ENSP00000445062.1:n.986-294_986-293insT
ENST00000539050.5:c.1082-294_1082-293insT	ENSP00000442343.2:n.1082-294_1082-293insT
ENST00000623108.3:c.1082-294_1082-293insT	ENSP00000485110.1:n.1082-294_1082-293insT
NM_000770.3:c.1292-294_1292-293insT MANE Select	NP_000761.3:n.1292-294_1292-293insT
NM_001198853.1:c.1082-294_1082-293insT	NP_001185782.1:n.1082-294_1082-293insT
NM_001198854.1:c.986-294_986-293insT	NP_001185783.1:n.986-294_986-293insT
NM_001198855.1:c.1082-294_1082-293insT	NP_001185784.1:n.1082-294_1082-293insT
XR_945610.1:n.1427-294_1427-293insT