Canonical Allele Identifier: CA2610269899

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037074-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037080_95037081del , CM000672.2:g.95037080_95037081del	GRCh38
NC_000010.10:g.96796837_96796838del , CM000672.1:g.96796837_96796838del	GRCh37
NC_000010.9:g.96786827_96786828del	NCBI36
NG_007972.1:g.37422_37423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*52_*53del MANE Select	ENSP00000360317.3:n.*52_*53del
ENST00000371270.5:c.*52_*53del	ENSP00000360317.3:n.*52_*53del
ENST00000490994.6:c.*1311_*1312del	ENSP00000433314.1:n.*1311_*1312del
ENST00000525991.5:c.*1100_*1101del	ENSP00000433842.1:n.*1100_*1101del
ENST00000526814.5:n.1780_1781del
ENST00000527420.5:c.*382_*383del	ENSP00000433191.1:n.*382_*383del
ENST00000527953.5:n.1819_1820del
ENST00000533320.5:n.1759_1760del
ENST00000535898.5:c.*52_*53del	ENSP00000445062.1:n.*52_*53del
ENST00000539050.5:c.*52_*53del	ENSP00000442343.2:n.*52_*53del
ENST00000623108.3:c.*52_*53del	ENSP00000485110.1:n.*52_*53del
NM_000770.3:c.*52_*53del MANE Select	NP_000761.3:n.*52_*53del
NM_001198853.1:c.*52_*53del	NP_001185782.1:n.*52_*53del
NM_001198854.1:c.*52_*53del	NP_001185783.1:n.*52_*53del
NM_001198855.1:c.*52_*53del	NP_001185784.1:n.*52_*53del