Canonical Allele Identifier: CA931394178
Gene: CYP2C8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95049243_95049244del , CM000672.2:g.95049243_95049244del GRCh38
NC_000010.10:g.96809000_96809001del , CM000672.1:g.96809000_96809001del GRCh37
NC_000010.9:g.96798990_96798991del NCBI36
NG_007972.1:g.25256_25257del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371270.6:c.820-3291_820-3290del MANE Select ENSP00000360317.3:n.820-3291_820-3290del
ENST00000371270.5:c.820-3291_820-3290del ENSP00000360317.3:n.820-3291_820-3290del
ENST00000479946.2:n.1124-3291_1124-3290del
ENST00000490994.6:c.*606-3291_*606-3290del ENSP00000433314.1:n.*606-3291_*606-3290del
ENST00000525991.5:c.*395-3291_*395-3290del ENSP00000433842.1:n.*395-3291_*395-3290del
ENST00000526814.5:n.1075-3291_1075-3290del
ENST00000527420.5:c.820-3291_820-3290del ENSP00000433191.1:n.820-3291_820-3290del
ENST00000527953.5:n.1075-3291_1075-3290del
ENST00000533320.5:n.1054-3291_1054-3290del
ENST00000535898.5:c.514-3291_514-3290del ENSP00000445062.1:n.514-3291_514-3290del
ENST00000539050.5:c.610-3291_610-3290del ENSP00000442343.2:n.610-3291_610-3290del
ENST00000623108.3:c.610-3291_610-3290del ENSP00000485110.1:n.610-3291_610-3290del
ENST00000628935.1:c.562-3291_562-3290del ENSP00000487145.1:n.562-3291_562-3290del
NM_000770.3:c.820-3291_820-3290del MANE Select NP_000761.3:n.820-3291_820-3290del
NM_001198853.1:c.610-3291_610-3290del NP_001185782.1:n.610-3291_610-3290del
NM_001198854.1:c.514-3291_514-3290del NP_001185783.1:n.514-3291_514-3290del
NM_001198855.1:c.610-3291_610-3290del NP_001185784.1:n.610-3291_610-3290del
XR_945610.1:n.916-3291_916-3290del