Canonical Allele Identifier: CA2789075234
Gene: CYP2C8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95067361_95067362insAAAAAAA , CM000672.2:g.95067361_95067362insAAAAAAA GRCh38
NC_000010.10:g.96827118_96827119insAAAAAAA , CM000672.1:g.96827118_96827119insAAAAAAA GRCh37
NC_000010.9:g.96817108_96817109insAAAAAAA NCBI36
NG_007972.1:g.7138_7139insTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371270.6:c.332-3_332-2insTTTTTTT MANE Select ENSP00000360317.3:n.332-3_332-2insTTTTTTT
ENST00000371270.5:c.332-3_332-2insTTTTTTT ENSP00000360317.3:n.332-3_332-2insTTTTTTT
ENST00000479946.2:n.633_634insTTTTTTT
ENST00000490994.6:c.*118-3_*118-2insTTTTTTT ENSP00000433314.1:n.*118-3_*118-2insTTTTTTT
ENST00000525991.5:c.207-3_207-2insTTTTTTT ENSP00000433842.1:n.207-3_207-2insTTTTTTT
ENST00000526814.5:n.584_585insTTTTTTT
ENST00000527420.5:c.332-3_332-2insTTTTTTT ENSP00000433191.1:n.332-3_332-2insTTTTTTT
ENST00000527953.5:n.584_585insTTTTTTT
ENST00000533320.5:n.563_564insTTTTTTT
ENST00000535898.5:c.26-3_26-2insTTTTTTT ENSP00000445062.1:n.26-3_26-2insTTTTTTT
ENST00000539050.5:c.122-3_122-2insTTTTTTT ENSP00000442343.2:n.122-3_122-2insTTTTTTT
ENST00000623108.3:c.122-3_122-2insTTTTTTT ENSP00000485110.1:n.122-3_122-2insTTTTTTT
ENST00000628935.1:c.71_72insTTTTTTT ENSP00000487145.1:p.Leu24PhefsTer?
NM_000770.3:c.332-3_332-2insTTTTTTT MANE Select NP_000761.3:n.332-3_332-2insTTTTTTT
NM_001198853.1:c.122-3_122-2insTTTTTTT NP_001185782.1:n.122-3_122-2insTTTTTTT
NM_001198854.1:c.26-3_26-2insTTTTTTT NP_001185783.1:n.26-3_26-2insTTTTTTT
NM_001198855.1:c.122-3_122-2insTTTTTTT NP_001185784.1:n.122-3_122-2insTTTTTTT
XR_945610.1:n.428-3_428-2insTTTTTTT