Canonical Allele Identifier: CA931394091

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2033165472
• gnomAD v3: 10-95049127-C-CAG
• gnomAD v4: 10-95049127-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95049127_95049128insAG , CM000672.2:g.95049127_95049128insAG	GRCh38
NC_000010.10:g.96808884_96808885insAG , CM000672.1:g.96808884_96808885insAG	GRCh37
NC_000010.9:g.96798874_96798875insAG	NCBI36
NG_007972.1:g.25370_25371insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.820-3177_820-3176insCT MANE Select	ENSP00000360317.3:n.820-3177_820-3176insCT
ENST00000371270.5:c.820-3177_820-3176insCT	ENSP00000360317.3:n.820-3177_820-3176insCT
ENST00000479946.2:n.1124-3177_1124-3176insCT
ENST00000490994.6:c.*606-3177_*606-3176insCT	ENSP00000433314.1:n.*606-3177_*606-3176insCT
ENST00000525991.5:c.*395-3177_*395-3176insCT	ENSP00000433842.1:n.*395-3177_*395-3176insCT
ENST00000526814.5:n.1075-3177_1075-3176insCT
ENST00000527420.5:c.820-3177_820-3176insCT	ENSP00000433191.1:n.820-3177_820-3176insCT
ENST00000527953.5:n.1075-3177_1075-3176insCT
ENST00000533320.5:n.1054-3177_1054-3176insCT
ENST00000535898.5:c.514-3177_514-3176insCT	ENSP00000445062.1:n.514-3177_514-3176insCT
ENST00000539050.5:c.610-3177_610-3176insCT	ENSP00000442343.2:n.610-3177_610-3176insCT
ENST00000623108.3:c.610-3177_610-3176insCT	ENSP00000485110.1:n.610-3177_610-3176insCT
ENST00000628935.1:c.562-3177_562-3176insCT	ENSP00000487145.1:n.562-3177_562-3176insCT
NM_000770.3:c.820-3177_820-3176insCT MANE Select	NP_000761.3:n.820-3177_820-3176insCT
NM_001198853.1:c.610-3177_610-3176insCT	NP_001185782.1:n.610-3177_610-3176insCT
NM_001198854.1:c.514-3177_514-3176insCT	NP_001185783.1:n.514-3177_514-3176insCT
NM_001198855.1:c.610-3177_610-3176insCT	NP_001185784.1:n.610-3177_610-3176insCT
XR_945610.1:n.916-3177_916-3176insCT