Canonical Allele Identifier: CA2516116939

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037125del , CM000672.2:g.95037125del	GRCh38
NC_000010.10:g.96796882del , CM000672.1:g.96796882del	GRCh37
NC_000010.9:g.96786872del	NCBI36
NG_007972.1:g.37374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*4del MANE Select	ENSP00000360317.3:n.*4del
ENST00000371270.5:c.*4del	ENSP00000360317.3:n.*4del
ENST00000490994.6:c.*1263del	ENSP00000433314.1:n.*1263del
ENST00000525991.5:c.*1052del	ENSP00000433842.1:n.*1052del
ENST00000526814.5:n.1732del
ENST00000527420.5:c.*334del	ENSP00000433191.1:n.*334del
ENST00000527953.5:n.1771del
ENST00000533320.5:n.1711del
ENST00000535898.5:c.*4del	ENSP00000445062.1:n.*4del
ENST00000539050.5:c.*4del	ENSP00000442343.2:n.*4del
ENST00000623108.3:c.*4del	ENSP00000485110.1:n.*4del
NM_000770.3:c.*4del MANE Select	NP_000761.3:n.*4del
NM_001198853.1:c.*4del	NP_001185782.1:n.*4del
NM_001198854.1:c.*4del	NP_001185783.1:n.*4del
NM_001198855.1:c.*4del	NP_001185784.1:n.*4del