Canonical Allele Identifier: CA670231301

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1252786705
• gnomAD v3: 10-95048977-TTAAAC-T
• gnomAD v4: 10-95048977-TTAAAC-T
• MyVariant Identifiers: chr10:g.96808735_96808739del (hg19) ; chr10:g.95048978_95048982del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95048982_95048986del , CM000672.2:g.95048982_95048986del	GRCh38
NC_000010.10:g.96808739_96808743del , CM000672.1:g.96808739_96808743del	GRCh37
NC_000010.9:g.96798729_96798733del	NCBI36
NG_007972.1:g.25516_25520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.820-3031_820-3027del MANE Select	ENSP00000360317.3:n.820-3031_820-3027del
ENST00000371270.5:c.820-3031_820-3027del	ENSP00000360317.3:n.820-3031_820-3027del
ENST00000479946.2:n.1124-3031_1124-3027del
ENST00000490994.6:c.*606-3031_*606-3027del	ENSP00000433314.1:n.*606-3031_*606-3027del
ENST00000525991.5:c.*395-3031_*395-3027del	ENSP00000433842.1:n.*395-3031_*395-3027del
ENST00000526814.5:n.1075-3031_1075-3027del
ENST00000527420.5:c.820-3031_820-3027del	ENSP00000433191.1:n.820-3031_820-3027del
ENST00000527953.5:n.1075-3031_1075-3027del
ENST00000533320.5:n.1054-3031_1054-3027del
ENST00000535898.5:c.514-3031_514-3027del	ENSP00000445062.1:n.514-3031_514-3027del
ENST00000539050.5:c.610-3031_610-3027del	ENSP00000442343.2:n.610-3031_610-3027del
ENST00000623108.3:c.610-3031_610-3027del	ENSP00000485110.1:n.610-3031_610-3027del
ENST00000628935.1:c.562-3031_562-3027del	ENSP00000487145.1:n.562-3031_562-3027del
NM_000770.3:c.820-3031_820-3027del MANE Select	NP_000761.3:n.820-3031_820-3027del
NM_001198853.1:c.610-3031_610-3027del	NP_001185782.1:n.610-3031_610-3027del
NM_001198854.1:c.514-3031_514-3027del	NP_001185783.1:n.514-3031_514-3027del
NM_001198855.1:c.610-3031_610-3027del	NP_001185784.1:n.610-3031_610-3027del
XR_945610.1:n.916-3031_916-3027del