Canonical Allele Identifier: CA470841251

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1233430553
• MyVariant Identifiers: chr10:g.96797060del (hg19) ; chr10:g.95037303del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037303del , CM000672.2:g.95037303del	GRCh38
NC_000010.10:g.96797060del , CM000672.1:g.96797060del	GRCh37
NC_000010.9:g.96787050del	NCBI36
NG_007972.1:g.37195del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1298del MANE Select	ENSP00000360317.3:p.Arg433GlnfsTer17
ENST00000371270.5:c.1298del	ENSP00000360317.3:p.Arg433GlnfsTer17
ENST00000490994.6:c.*1084del	ENSP00000433314.1:n.*1084del
ENST00000525991.5:c.*873del	ENSP00000433842.1:n.*873del
ENST00000526814.5:n.1553del
ENST00000527420.5:c.*155del	ENSP00000433191.1:n.*155del
ENST00000527953.5:n.1592del
ENST00000531714.1:n.486del
ENST00000533320.5:n.1532del
ENST00000535898.5:c.992del	ENSP00000445062.1:p.Arg331GlnfsTer17
ENST00000539050.5:c.1088del	ENSP00000442343.2:p.Arg363GlnfsTer17
ENST00000623108.3:c.1088del	ENSP00000485110.1:p.Arg363GlnfsTer17
NM_000770.3:c.1298del MANE Select	NP_000761.3:p.Arg433GlnfsTer17
NM_001198853.1:c.1088del	NP_001185782.1:p.Arg363GlnfsTer17
NM_001198854.1:c.992del	NP_001185783.1:p.Arg331GlnfsTer17
NM_001198855.1:c.1088del	NP_001185784.1:p.Arg363GlnfsTer17
XR_945610.1:n.1433del