Canonical Allele Identifier: CA1929375932

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2032911813

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037595_95037598dup , CM000672.2:g.95037595_95037598dup	GRCh38
NC_000010.10:g.96797352_96797355dup , CM000672.1:g.96797352_96797355dup	GRCh37
NC_000010.9:g.96787342_96787345dup	NCBI36
NG_007972.1:g.36902_36905dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-287_1292-284dup MANE Select	ENSP00000360317.3:n.1292-287_1292-284dup
ENST00000371270.5:c.1292-287_1292-284dup	ENSP00000360317.3:n.1292-287_1292-284dup
ENST00000490994.6:c.*1078-287_*1078-284dup	ENSP00000433314.1:n.*1078-287_*1078-284dup
ENST00000525991.5:c.*867-287_*867-284dup	ENSP00000433842.1:n.*867-287_*867-284dup
ENST00000526814.5:n.1547-287_1547-284dup
ENST00000527420.5:c.*149-287_*149-284dup	ENSP00000433191.1:n.*149-287_*149-284dup
ENST00000527953.5:n.1586-287_1586-284dup
ENST00000531714.1:n.480-287_480-284dup
ENST00000533320.5:n.1526-287_1526-284dup
ENST00000535898.5:c.986-287_986-284dup	ENSP00000445062.1:n.986-287_986-284dup
ENST00000539050.5:c.1082-287_1082-284dup	ENSP00000442343.2:n.1082-287_1082-284dup
ENST00000623108.3:c.1082-287_1082-284dup	ENSP00000485110.1:n.1082-287_1082-284dup
NM_000770.3:c.1292-287_1292-284dup MANE Select	NP_000761.3:n.1292-287_1292-284dup
NM_001198853.1:c.1082-287_1082-284dup	NP_001185782.1:n.1082-287_1082-284dup
NM_001198854.1:c.986-287_986-284dup	NP_001185783.1:n.986-287_986-284dup
NM_001198855.1:c.1082-287_1082-284dup	NP_001185784.1:n.1082-287_1082-284dup
XR_945610.1:n.1427-287_1427-284dup