Canonical Allele Identifier: CA931389152

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2032908489
• gnomAD v3: 10-95037445-GATGA-G
• gnomAD v4: 10-95037445-GATGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037449_95037452del , CM000672.2:g.95037449_95037452del	GRCh38
NC_000010.10:g.96797206_96797209del , CM000672.1:g.96797206_96797209del	GRCh37
NC_000010.9:g.96787196_96787199del	NCBI36
NG_007972.1:g.37049_37052del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1292-140_1292-137del MANE Select	ENSP00000360317.3:n.1292-140_1292-137del
ENST00000371270.5:c.1292-140_1292-137del	ENSP00000360317.3:n.1292-140_1292-137del
ENST00000490994.6:c.*1078-140_*1078-137del	ENSP00000433314.1:n.*1078-140_*1078-137del
ENST00000525991.5:c.*867-140_*867-137del	ENSP00000433842.1:n.*867-140_*867-137del
ENST00000526814.5:n.1547-140_1547-137del
ENST00000527420.5:c.*149-140_*149-137del	ENSP00000433191.1:n.*149-140_*149-137del
ENST00000527953.5:n.1586-140_1586-137del
ENST00000531714.1:n.480-140_480-137del
ENST00000533320.5:n.1526-140_1526-137del
ENST00000535898.5:c.986-140_986-137del	ENSP00000445062.1:n.986-140_986-137del
ENST00000539050.5:c.1082-140_1082-137del	ENSP00000442343.2:n.1082-140_1082-137del
ENST00000623108.3:c.1082-140_1082-137del	ENSP00000485110.1:n.1082-140_1082-137del
NM_000770.3:c.1292-140_1292-137del MANE Select	NP_000761.3:n.1292-140_1292-137del
NM_001198853.1:c.1082-140_1082-137del	NP_001185782.1:n.1082-140_1082-137del
NM_001198854.1:c.986-140_986-137del	NP_001185783.1:n.986-140_986-137del
NM_001198855.1:c.1082-140_1082-137del	NP_001185784.1:n.1082-140_1082-137del
XR_945610.1:n.1427-140_1427-137del