Canonical Allele Identifier: CA2789074432

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037085_95037090del , CM000672.2:g.95037085_95037090del	GRCh38
NC_000010.10:g.96796842_96796847del , CM000672.1:g.96796842_96796847del	GRCh37
NC_000010.9:g.96786832_96786837del	NCBI36
NG_007972.1:g.37410_37415del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*40_*45del MANE Select	ENSP00000360317.3:n.*40_*45del
ENST00000371270.5:c.*40_*45del	ENSP00000360317.3:n.*40_*45del
ENST00000490994.6:c.*1299_*1304del	ENSP00000433314.1:n.*1299_*1304del
ENST00000525991.5:c.*1088_*1093del	ENSP00000433842.1:n.*1088_*1093del
ENST00000526814.5:n.1768_1773del
ENST00000527420.5:c.*370_*375del	ENSP00000433191.1:n.*370_*375del
ENST00000527953.5:n.1807_1812del
ENST00000533320.5:n.1747_1752del
ENST00000535898.5:c.*40_*45del	ENSP00000445062.1:n.*40_*45del
ENST00000539050.5:c.*40_*45del	ENSP00000442343.2:n.*40_*45del
ENST00000623108.3:c.*40_*45del	ENSP00000485110.1:n.*40_*45del
NM_000770.3:c.*40_*45del MANE Select	NP_000761.3:n.*40_*45del
NM_001198853.1:c.*40_*45del	NP_001185782.1:n.*40_*45del
NM_001198854.1:c.*40_*45del	NP_001185783.1:n.*40_*45del
NM_001198855.1:c.*40_*45del	NP_001185784.1:n.*40_*45del