Canonical Allele Identifier: CA2789074448

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037732_95037733insCG , CM000672.2:g.95037732_95037733insCG	GRCh38
NC_000010.10:g.96797489_96797490insCG , CM000672.1:g.96797489_96797490insCG	GRCh37
NC_000010.9:g.96787479_96787480insCG	NCBI36
NG_007972.1:g.36765_36766insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-424_1292-423insCG MANE Select	ENSP00000360317.3:n.1292-424_1292-423insCG
ENST00000371270.5:c.1292-424_1292-423insCG	ENSP00000360317.3:n.1292-424_1292-423insCG
ENST00000490994.6:c.*1078-424_*1078-423insCG	ENSP00000433314.1:n.*1078-424_*1078-423insCG
ENST00000525991.5:c.*867-424_*867-423insCG	ENSP00000433842.1:n.*867-424_*867-423insCG
ENST00000526814.5:n.1547-424_1547-423insCG
ENST00000527420.5:c.*149-424_*149-423insCG	ENSP00000433191.1:n.*149-424_*149-423insCG
ENST00000527953.5:n.1586-424_1586-423insCG
ENST00000531714.1:n.480-424_480-423insCG
ENST00000533320.5:n.1526-424_1526-423insCG
ENST00000535898.5:c.986-424_986-423insCG	ENSP00000445062.1:n.986-424_986-423insCG
ENST00000539050.5:c.1082-424_1082-423insCG	ENSP00000442343.2:n.1082-424_1082-423insCG
ENST00000623108.3:c.1082-424_1082-423insCG	ENSP00000485110.1:n.1082-424_1082-423insCG
NM_000770.3:c.1292-424_1292-423insCG MANE Select	NP_000761.3:n.1292-424_1292-423insCG
NM_001198853.1:c.1082-424_1082-423insCG	NP_001185782.1:n.1082-424_1082-423insCG
NM_001198854.1:c.986-424_986-423insCG	NP_001185783.1:n.986-424_986-423insCG
NM_001198855.1:c.1082-424_1082-423insCG	NP_001185784.1:n.1082-424_1082-423insCG
XR_945610.1:n.1427-424_1427-423insCG