Canonical Allele Identifier: CA2610269869

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037021-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037024del , CM000672.2:g.95037024del	GRCh38
NC_000010.10:g.96796781del , CM000672.1:g.96796781del	GRCh37
NC_000010.9:g.96786771del	NCBI36
NG_007972.1:g.37476del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*106del MANE Select	ENSP00000360317.3:n.*106del
ENST00000371270.5:c.*106del	ENSP00000360317.3:n.*106del
ENST00000490994.6:c.*1365del	ENSP00000433314.1:n.*1365del
ENST00000525991.5:c.*1154del	ENSP00000433842.1:n.*1154del
ENST00000526814.5:n.1834del
ENST00000527420.5:c.*436del	ENSP00000433191.1:n.*436del
ENST00000527953.5:n.1873del
ENST00000533320.5:n.1813del
ENST00000535898.5:c.*106del	ENSP00000445062.1:n.*106del
ENST00000539050.5:c.*106del	ENSP00000442343.2:n.*106del
ENST00000623108.3:c.*106del	ENSP00000485110.1:n.*106del
NM_000770.3:c.*106del MANE Select	NP_000761.3:n.*106del
NM_001198853.1:c.*106del	NP_001185782.1:n.*106del
NM_001198854.1:c.*106del	NP_001185783.1:n.*106del
NM_001198855.1:c.*106del	NP_001185784.1:n.*106del