Canonical Allele Identifier: CA1929375770

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2032909571

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037492_95037493insGCCTTT , CM000672.2:g.95037492_95037493insGCCTTT	GRCh38
NC_000010.10:g.96797249_96797250insGCCTTT , CM000672.1:g.96797249_96797250insGCCTTT	GRCh37
NC_000010.9:g.96787239_96787240insGCCTTT	NCBI36
NG_007972.1:g.37005_37006insAAAGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-184_1292-183insAAAGGC MANE Select	ENSP00000360317.3:n.1292-184_1292-183insAAAGGC
ENST00000371270.5:c.1292-184_1292-183insAAAGGC	ENSP00000360317.3:n.1292-184_1292-183insAAAGGC
ENST00000490994.6:c.*1078-184_*1078-183insAAAGGC	ENSP00000433314.1:n.*1078-184_*1078-183insAAAGGC
ENST00000525991.5:c.*867-184_*867-183insAAAGGC	ENSP00000433842.1:n.*867-184_*867-183insAAAGGC
ENST00000526814.5:n.1547-184_1547-183insAAAGGC
ENST00000527420.5:c.*149-184_*149-183insAAAGGC	ENSP00000433191.1:n.*149-184_*149-183insAAAGGC
ENST00000527953.5:n.1586-184_1586-183insAAAGGC
ENST00000531714.1:n.480-184_480-183insAAAGGC
ENST00000533320.5:n.1526-184_1526-183insAAAGGC
ENST00000535898.5:c.986-184_986-183insAAAGGC	ENSP00000445062.1:n.986-184_986-183insAAAGGC
ENST00000539050.5:c.1082-184_1082-183insAAAGGC	ENSP00000442343.2:n.1082-184_1082-183insAAAGGC
ENST00000623108.3:c.1082-184_1082-183insAAAGGC	ENSP00000485110.1:n.1082-184_1082-183insAAAGGC
NM_000770.3:c.1292-184_1292-183insAAAGGC MANE Select	NP_000761.3:n.1292-184_1292-183insAAAGGC
NM_001198853.1:c.1082-184_1082-183insAAAGGC	NP_001185782.1:n.1082-184_1082-183insAAAGGC
NM_001198854.1:c.986-184_986-183insAAAGGC	NP_001185783.1:n.986-184_986-183insAAAGGC
NM_001198855.1:c.1082-184_1082-183insAAAGGC	NP_001185784.1:n.1082-184_1082-183insAAAGGC
XR_945610.1:n.1427-184_1427-183insAAAGGC