Canonical Allele Identifier: CA2610269891

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037059-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037062del , CM000672.2:g.95037062del	GRCh38
NC_000010.10:g.96796819del , CM000672.1:g.96796819del	GRCh37
NC_000010.9:g.96786809del	NCBI36
NG_007972.1:g.37438del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*68del MANE Select	ENSP00000360317.3:n.*68del
ENST00000371270.5:c.*68del	ENSP00000360317.3:n.*68del
ENST00000490994.6:c.*1327del	ENSP00000433314.1:n.*1327del
ENST00000525991.5:c.*1116del	ENSP00000433842.1:n.*1116del
ENST00000526814.5:n.1796del
ENST00000527420.5:c.*398del	ENSP00000433191.1:n.*398del
ENST00000527953.5:n.1835del
ENST00000533320.5:n.1775del
ENST00000535898.5:c.*68del	ENSP00000445062.1:n.*68del
ENST00000539050.5:c.*68del	ENSP00000442343.2:n.*68del
ENST00000623108.3:c.*68del	ENSP00000485110.1:n.*68del
NM_000770.3:c.*68del MANE Select	NP_000761.3:n.*68del
NM_001198853.1:c.*68del	NP_001185782.1:n.*68del
NM_001198854.1:c.*68del	NP_001185783.1:n.*68del
NM_001198855.1:c.*68del	NP_001185784.1:n.*68del