Canonical Allele Identifier: CA670231283

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1159945625
• MyVariant Identifiers: chr10:g.96808719_96808720insA (hg19) ; chr10:g.95048962_95048963insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95048963dup , CM000672.2:g.95048963dup	GRCh38
NC_000010.10:g.96808720dup , CM000672.1:g.96808720dup	GRCh37
NC_000010.9:g.96798710dup	NCBI36
NG_007972.1:g.25535dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.820-3012dup MANE Select	ENSP00000360317.3:n.820-3012dup
ENST00000371270.5:c.820-3012dup	ENSP00000360317.3:n.820-3012dup
ENST00000479946.2:n.1124-3012dup
ENST00000490994.6:c.*606-3012dup	ENSP00000433314.1:n.*606-3012dup
ENST00000525991.5:c.*395-3012dup	ENSP00000433842.1:n.*395-3012dup
ENST00000526814.5:n.1075-3012dup
ENST00000527420.5:c.820-3012dup	ENSP00000433191.1:n.820-3012dup
ENST00000527953.5:n.1075-3012dup
ENST00000533320.5:n.1054-3012dup
ENST00000535898.5:c.514-3012dup	ENSP00000445062.1:n.514-3012dup
ENST00000539050.5:c.610-3012dup	ENSP00000442343.2:n.610-3012dup
ENST00000623108.3:c.610-3012dup	ENSP00000485110.1:n.610-3012dup
ENST00000628935.1:c.562-3012dup	ENSP00000487145.1:n.562-3012dup
NM_000770.3:c.820-3012dup MANE Select	NP_000761.3:n.820-3012dup
NM_001198853.1:c.610-3012dup	NP_001185782.1:n.610-3012dup
NM_001198854.1:c.514-3012dup	NP_001185783.1:n.514-3012dup
NM_001198855.1:c.610-3012dup	NP_001185784.1:n.610-3012dup
XR_945610.1:n.916-3012dup