Canonical Allele Identifier: CA1929368529
Gene: CYP2C8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95051218_95051219delinsTG , CM000672.2:g.95051218_95051219delinsTG GRCh38
NC_000010.10:g.96810975_96810976delinsTG , CM000672.1:g.96810975_96810976delinsTG GRCh37
NC_000010.9:g.96800965_96800966delinsTG NCBI36
NG_007972.1:g.23279_23280delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371270.6:c.820-5268_820-5267delinsCA MANE Select ENSP00000360317.3:n.820-5268_820-5267delinsCA
ENST00000371270.5:c.820-5268_820-5267delinsCA ENSP00000360317.3:n.820-5268_820-5267delinsCA
ENST00000479946.2:n.1124-5268_1124-5267delinsCA
ENST00000490994.6:c.*606-5268_*606-5267delinsCA ENSP00000433314.1:n.*606-5268_*606-5267delinsCA
ENST00000525991.5:c.*395-5268_*395-5267delinsCA ENSP00000433842.1:n.*395-5268_*395-5267delinsCA
ENST00000526814.5:n.1075-5268_1075-5267delinsCA
ENST00000527420.5:c.820-5268_820-5267delinsCA ENSP00000433191.1:n.820-5268_820-5267delinsCA
ENST00000527953.5:n.1075-5268_1075-5267delinsCA
ENST00000533320.5:n.1054-5268_1054-5267delinsCA
ENST00000535898.5:c.514-5268_514-5267delinsCA ENSP00000445062.1:n.514-5268_514-5267delinsCA
ENST00000539050.5:c.610-5268_610-5267delinsCA ENSP00000442343.2:n.610-5268_610-5267delinsCA
ENST00000623108.3:c.610-5268_610-5267delinsCA ENSP00000485110.1:n.610-5268_610-5267delinsCA
ENST00000628935.1:c.562-5268_562-5267delinsCA ENSP00000487145.1:n.562-5268_562-5267delinsCA
NM_000770.3:c.820-5268_820-5267delinsCA MANE Select NP_000761.3:n.820-5268_820-5267delinsCA
NM_001198853.1:c.610-5268_610-5267delinsCA NP_001185782.1:n.610-5268_610-5267delinsCA
NM_001198854.1:c.514-5268_514-5267delinsCA NP_001185783.1:n.514-5268_514-5267delinsCA
NM_001198855.1:c.610-5268_610-5267delinsCA NP_001185784.1:n.610-5268_610-5267delinsCA
XR_945610.1:n.916-5268_916-5267delinsCA