Canonical Allele Identifier: CA931394222
Gene: CYP2C8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95049246_95049247insTGATACG , CM000672.2:g.95049246_95049247insTGATACG GRCh38
NC_000010.10:g.96809003_96809004insTGATACG , CM000672.1:g.96809003_96809004insTGATACG GRCh37
NC_000010.9:g.96798993_96798994insTGATACG NCBI36
NG_007972.1:g.25251_25252insCGTATCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371270.6:c.820-3296_820-3295insCGTATCA MANE Select ENSP00000360317.3:n.820-3296_820-3295insCGTATCA
ENST00000371270.5:c.820-3296_820-3295insCGTATCA ENSP00000360317.3:n.820-3296_820-3295insCGTATCA
ENST00000479946.2:n.1124-3296_1124-3295insCGTATCA
ENST00000490994.6:c.*606-3296_*606-3295insCGTATCA ENSP00000433314.1:n.*606-3296_*606-3295insCGTATCA
ENST00000525991.5:c.*395-3296_*395-3295insCGTATCA ENSP00000433842.1:n.*395-3296_*395-3295insCGTATCA
ENST00000526814.5:n.1075-3296_1075-3295insCGTATCA
ENST00000527420.5:c.820-3296_820-3295insCGTATCA ENSP00000433191.1:n.820-3296_820-3295insCGTATCA
ENST00000527953.5:n.1075-3296_1075-3295insCGTATCA
ENST00000533320.5:n.1054-3296_1054-3295insCGTATCA
ENST00000535898.5:c.514-3296_514-3295insCGTATCA ENSP00000445062.1:n.514-3296_514-3295insCGTATCA
ENST00000539050.5:c.610-3296_610-3295insCGTATCA ENSP00000442343.2:n.610-3296_610-3295insCGTATCA
ENST00000623108.3:c.610-3296_610-3295insCGTATCA ENSP00000485110.1:n.610-3296_610-3295insCGTATCA
ENST00000628935.1:c.562-3296_562-3295insCGTATCA ENSP00000487145.1:n.562-3296_562-3295insCGTATCA
NM_000770.3:c.820-3296_820-3295insCGTATCA MANE Select NP_000761.3:n.820-3296_820-3295insCGTATCA
NM_001198853.1:c.610-3296_610-3295insCGTATCA NP_001185782.1:n.610-3296_610-3295insCGTATCA
NM_001198854.1:c.514-3296_514-3295insCGTATCA NP_001185783.1:n.514-3296_514-3295insCGTATCA
NM_001198855.1:c.610-3296_610-3295insCGTATCA NP_001185784.1:n.610-3296_610-3295insCGTATCA
XR_945610.1:n.916-3296_916-3295insCGTATCA