Canonical Allele Identifier: CA2610269936

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037342-CTTGTGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037345_95037350del , CM000672.2:g.95037345_95037350del	GRCh38
NC_000010.10:g.96797102_96797107del , CM000672.1:g.96797102_96797107del	GRCh37
NC_000010.9:g.96787092_96787097del	NCBI36
NG_007972.1:g.37150_37155del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-39_1292-34del MANE Select	ENSP00000360317.3:n.1292-39_1292-34del
ENST00000371270.5:c.1292-39_1292-34del	ENSP00000360317.3:n.1292-39_1292-34del
ENST00000490994.6:c.*1078-39_*1078-34del	ENSP00000433314.1:n.*1078-39_*1078-34del
ENST00000525991.5:c.*867-39_*867-34del	ENSP00000433842.1:n.*867-39_*867-34del
ENST00000526814.5:n.1547-39_1547-34del
ENST00000527420.5:c.*149-39_*149-34del	ENSP00000433191.1:n.*149-39_*149-34del
ENST00000527953.5:n.1586-39_1586-34del
ENST00000531714.1:n.480-39_480-34del
ENST00000533320.5:n.1526-39_1526-34del
ENST00000535898.5:c.986-39_986-34del	ENSP00000445062.1:n.986-39_986-34del
ENST00000539050.5:c.1082-39_1082-34del	ENSP00000442343.2:n.1082-39_1082-34del
ENST00000623108.3:c.1082-39_1082-34del	ENSP00000485110.1:n.1082-39_1082-34del
NM_000770.3:c.1292-39_1292-34del MANE Select	NP_000761.3:n.1292-39_1292-34del
NM_001198853.1:c.1082-39_1082-34del	NP_001185782.1:n.1082-39_1082-34del
NM_001198854.1:c.986-39_986-34del	NP_001185783.1:n.986-39_986-34del
NM_001198855.1:c.1082-39_1082-34del	NP_001185784.1:n.1082-39_1082-34del
XR_945610.1:n.1427-39_1427-34del