Canonical Allele Identifier: CA1929375701

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037445_95037449delinsGATGA , CM000672.2:g.95037445_95037449delinsGATGA	GRCh38
NC_000010.10:g.96797202_96797206delinsGATGA , CM000672.1:g.96797202_96797206delinsGATGA	GRCh37
NC_000010.9:g.96787192_96787196delinsGATGA	NCBI36
NG_007972.1:g.37049_37053delinsTCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-140_1292-136delinsTCATC MANE Select	ENSP00000360317.3:n.1292-140_1292-136delinsTCATC
ENST00000371270.5:c.1292-140_1292-136delinsTCATC	ENSP00000360317.3:n.1292-140_1292-136delinsTCATC
ENST00000490994.6:c.*1078-140_*1078-136delinsTCATC	ENSP00000433314.1:n.*1078-140_*1078-136delinsTCATC
ENST00000525991.5:c.*867-140_*867-136delinsTCATC	ENSP00000433842.1:n.*867-140_*867-136delinsTCATC
ENST00000526814.5:n.1547-140_1547-136delinsTCATC
ENST00000527420.5:c.*149-140_*149-136delinsTCATC	ENSP00000433191.1:n.*149-140_*149-136delinsTCATC
ENST00000527953.5:n.1586-140_1586-136delinsTCATC
ENST00000531714.1:n.480-140_480-136delinsTCATC
ENST00000533320.5:n.1526-140_1526-136delinsTCATC
ENST00000535898.5:c.986-140_986-136delinsTCATC	ENSP00000445062.1:n.986-140_986-136delinsTCATC
ENST00000539050.5:c.1082-140_1082-136delinsTCATC	ENSP00000442343.2:n.1082-140_1082-136delinsTCATC
ENST00000623108.3:c.1082-140_1082-136delinsTCATC	ENSP00000485110.1:n.1082-140_1082-136delinsTCATC
NM_000770.3:c.1292-140_1292-136delinsTCATC MANE Select	NP_000761.3:n.1292-140_1292-136delinsTCATC
NM_001198853.1:c.1082-140_1082-136delinsTCATC	NP_001185782.1:n.1082-140_1082-136delinsTCATC
NM_001198854.1:c.986-140_986-136delinsTCATC	NP_001185783.1:n.986-140_986-136delinsTCATC
NM_001198855.1:c.1082-140_1082-136delinsTCATC	NP_001185784.1:n.1082-140_1082-136delinsTCATC
XR_945610.1:n.1427-140_1427-136delinsTCATC