Canonical Allele Identifier: CA1929375941

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037602_95037606delinsCTTTA , CM000672.2:g.95037602_95037606delinsCTTTA	GRCh38
NC_000010.10:g.96797359_96797363delinsCTTTA , CM000672.1:g.96797359_96797363delinsCTTTA	GRCh37
NC_000010.9:g.96787349_96787353delinsCTTTA	NCBI36
NG_007972.1:g.36892_36896delinsTAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-297_1292-293delinsTAAAG MANE Select	ENSP00000360317.3:n.1292-297_1292-293delinsTAAAG
ENST00000371270.5:c.1292-297_1292-293delinsTAAAG	ENSP00000360317.3:n.1292-297_1292-293delinsTAAAG
ENST00000490994.6:c.*1078-297_*1078-293delinsTAAAG	ENSP00000433314.1:n.*1078-297_*1078-293delinsTAAAG
ENST00000525991.5:c.*867-297_*867-293delinsTAAAG	ENSP00000433842.1:n.*867-297_*867-293delinsTAAAG
ENST00000526814.5:n.1547-297_1547-293delinsTAAAG
ENST00000527420.5:c.*149-297_*149-293delinsTAAAG	ENSP00000433191.1:n.*149-297_*149-293delinsTAAAG
ENST00000527953.5:n.1586-297_1586-293delinsTAAAG
ENST00000531714.1:n.480-297_480-293delinsTAAAG
ENST00000533320.5:n.1526-297_1526-293delinsTAAAG
ENST00000535898.5:c.986-297_986-293delinsTAAAG	ENSP00000445062.1:n.986-297_986-293delinsTAAAG
ENST00000539050.5:c.1082-297_1082-293delinsTAAAG	ENSP00000442343.2:n.1082-297_1082-293delinsTAAAG
ENST00000623108.3:c.1082-297_1082-293delinsTAAAG	ENSP00000485110.1:n.1082-297_1082-293delinsTAAAG
NM_000770.3:c.1292-297_1292-293delinsTAAAG MANE Select	NP_000761.3:n.1292-297_1292-293delinsTAAAG
NM_001198853.1:c.1082-297_1082-293delinsTAAAG	NP_001185782.1:n.1082-297_1082-293delinsTAAAG
NM_001198854.1:c.986-297_986-293delinsTAAAG	NP_001185783.1:n.986-297_986-293delinsTAAAG
NM_001198855.1:c.1082-297_1082-293delinsTAAAG	NP_001185784.1:n.1082-297_1082-293delinsTAAAG
XR_945610.1:n.1427-297_1427-293delinsTAAAG