Canonical Allele Identifier: CA2610269951
Gene: CYP2C8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95037363_95037364insTC , CM000672.2:g.95037363_95037364insTC GRCh38
NC_000010.10:g.96797120_96797121insTC , CM000672.1:g.96797120_96797121insTC GRCh37
NC_000010.9:g.96787110_96787111insTC NCBI36
NG_007972.1:g.37134_37135insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371270.6:c.1292-55_1292-54insGA MANE Select ENSP00000360317.3:n.1292-55_1292-54insGA
ENST00000371270.5:c.1292-55_1292-54insGA ENSP00000360317.3:n.1292-55_1292-54insGA
ENST00000490994.6:c.*1078-55_*1078-54insGA ENSP00000433314.1:n.*1078-55_*1078-54insGA
ENST00000525991.5:c.*867-55_*867-54insGA ENSP00000433842.1:n.*867-55_*867-54insGA
ENST00000526814.5:n.1547-55_1547-54insGA
ENST00000527420.5:c.*149-55_*149-54insGA ENSP00000433191.1:n.*149-55_*149-54insGA
ENST00000527953.5:n.1586-55_1586-54insGA
ENST00000531714.1:n.480-55_480-54insGA
ENST00000533320.5:n.1526-55_1526-54insGA
ENST00000535898.5:c.986-55_986-54insGA ENSP00000445062.1:n.986-55_986-54insGA
ENST00000539050.5:c.1082-55_1082-54insGA ENSP00000442343.2:n.1082-55_1082-54insGA
ENST00000623108.3:c.1082-55_1082-54insGA ENSP00000485110.1:n.1082-55_1082-54insGA
NM_000770.3:c.1292-55_1292-54insGA MANE Select NP_000761.3:n.1292-55_1292-54insGA
NM_001198853.1:c.1082-55_1082-54insGA NP_001185782.1:n.1082-55_1082-54insGA
NM_001198854.1:c.986-55_986-54insGA NP_001185783.1:n.986-55_986-54insGA
NM_001198855.1:c.1082-55_1082-54insGA NP_001185784.1:n.1082-55_1082-54insGA
XR_945610.1:n.1427-55_1427-54insGA