Canonical Allele Identifier: CA2610269962

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037382-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037382_95037383insAA , CM000672.2:g.95037382_95037383insAA	GRCh38
NC_000010.10:g.96797139_96797140insAA , CM000672.1:g.96797139_96797140insAA	GRCh37
NC_000010.9:g.96787129_96787130insAA	NCBI36
NG_007972.1:g.37115_37116insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-74_1292-73insTT MANE Select	ENSP00000360317.3:n.1292-74_1292-73insTT
ENST00000371270.5:c.1292-74_1292-73insTT	ENSP00000360317.3:n.1292-74_1292-73insTT
ENST00000490994.6:c.*1078-74_*1078-73insTT	ENSP00000433314.1:n.*1078-74_*1078-73insTT
ENST00000525991.5:c.*867-74_*867-73insTT	ENSP00000433842.1:n.*867-74_*867-73insTT
ENST00000526814.5:n.1547-74_1547-73insTT
ENST00000527420.5:c.*149-74_*149-73insTT	ENSP00000433191.1:n.*149-74_*149-73insTT
ENST00000527953.5:n.1586-74_1586-73insTT
ENST00000531714.1:n.480-74_480-73insTT
ENST00000533320.5:n.1526-74_1526-73insTT
ENST00000535898.5:c.986-74_986-73insTT	ENSP00000445062.1:n.986-74_986-73insTT
ENST00000539050.5:c.1082-74_1082-73insTT	ENSP00000442343.2:n.1082-74_1082-73insTT
ENST00000623108.3:c.1082-74_1082-73insTT	ENSP00000485110.1:n.1082-74_1082-73insTT
NM_000770.3:c.1292-74_1292-73insTT MANE Select	NP_000761.3:n.1292-74_1292-73insTT
NM_001198853.1:c.1082-74_1082-73insTT	NP_001185782.1:n.1082-74_1082-73insTT
NM_001198854.1:c.986-74_986-73insTT	NP_001185783.1:n.986-74_986-73insTT
NM_001198855.1:c.1082-74_1082-73insTT	NP_001185784.1:n.1082-74_1082-73insTT
XR_945610.1:n.1427-74_1427-73insTT