Canonical Allele Identifier: CA2610269885

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037043-AGAGAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037044_95037049del , CM000672.2:g.95037044_95037049del	GRCh38
NC_000010.10:g.96796801_96796806del , CM000672.1:g.96796801_96796806del	GRCh37
NC_000010.9:g.96786791_96786796del	NCBI36
NG_007972.1:g.37449_37454del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*79_*84del MANE Select	ENSP00000360317.3:n.*79_*84del
ENST00000371270.5:c.*79_*84del	ENSP00000360317.3:n.*79_*84del
ENST00000490994.6:c.*1338_*1343del	ENSP00000433314.1:n.*1338_*1343del
ENST00000525991.5:c.*1127_*1132del	ENSP00000433842.1:n.*1127_*1132del
ENST00000526814.5:n.1807_1812del
ENST00000527420.5:c.*409_*414del	ENSP00000433191.1:n.*409_*414del
ENST00000527953.5:n.1846_1851del
ENST00000533320.5:n.1786_1791del
ENST00000535898.5:c.*79_*84del	ENSP00000445062.1:n.*79_*84del
ENST00000539050.5:c.*79_*84del	ENSP00000442343.2:n.*79_*84del
ENST00000623108.3:c.*79_*84del	ENSP00000485110.1:n.*79_*84del
NM_000770.3:c.*79_*84del MANE Select	NP_000761.3:n.*79_*84del
NM_001198853.1:c.*79_*84del	NP_001185782.1:n.*79_*84del
NM_001198854.1:c.*79_*84del	NP_001185783.1:n.*79_*84del
NM_001198855.1:c.*79_*84del	NP_001185784.1:n.*79_*84del