Canonical Allele Identifier: CA2610269909

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037094-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037095del , CM000672.2:g.95037095del	GRCh38
NC_000010.10:g.96796852del , CM000672.1:g.96796852del	GRCh37
NC_000010.9:g.96786842del	NCBI36
NG_007972.1:g.37403del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*33del MANE Select	ENSP00000360317.3:n.*33del
ENST00000371270.5:c.*33del	ENSP00000360317.3:n.*33del
ENST00000490994.6:c.*1292del	ENSP00000433314.1:n.*1292del
ENST00000525991.5:c.*1081del	ENSP00000433842.1:n.*1081del
ENST00000526814.5:n.1761del
ENST00000527420.5:c.*363del	ENSP00000433191.1:n.*363del
ENST00000527953.5:n.1800del
ENST00000533320.5:n.1740del
ENST00000535898.5:c.*33del	ENSP00000445062.1:n.*33del
ENST00000539050.5:c.*33del	ENSP00000442343.2:n.*33del
ENST00000623108.3:c.*33del	ENSP00000485110.1:n.*33del
NM_000770.3:c.*33del MANE Select	NP_000761.3:n.*33del
NM_001198853.1:c.*33del	NP_001185782.1:n.*33del
NM_001198854.1:c.*33del	NP_001185783.1:n.*33del
NM_001198855.1:c.*33del	NP_001185784.1:n.*33del