Canonical Allele Identifier: CA211711692

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1001618379
• MyVariant Identifiers: chr10:g.96797265_96797266del (hg19) ; chr10:g.95037508_95037509del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037511_95037512del , CM000672.2:g.95037511_95037512del	GRCh38
NC_000010.10:g.96797268_96797269del , CM000672.1:g.96797268_96797269del	GRCh37
NC_000010.9:g.96787258_96787259del	NCBI36
NG_007972.1:g.36989_36990del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-200_1292-199del MANE Select	ENSP00000360317.3:n.1292-200_1292-199del
ENST00000371270.5:c.1292-200_1292-199del	ENSP00000360317.3:n.1292-200_1292-199del
ENST00000490994.6:c.*1078-200_*1078-199del	ENSP00000433314.1:n.*1078-200_*1078-199del
ENST00000525991.5:c.*867-200_*867-199del	ENSP00000433842.1:n.*867-200_*867-199del
ENST00000526814.5:n.1547-200_1547-199del
ENST00000527420.5:c.*149-200_*149-199del	ENSP00000433191.1:n.*149-200_*149-199del
ENST00000527953.5:n.1586-200_1586-199del
ENST00000531714.1:n.480-200_480-199del
ENST00000533320.5:n.1526-200_1526-199del
ENST00000535898.5:c.986-200_986-199del	ENSP00000445062.1:n.986-200_986-199del
ENST00000539050.5:c.1082-200_1082-199del	ENSP00000442343.2:n.1082-200_1082-199del
ENST00000623108.3:c.1082-200_1082-199del	ENSP00000485110.1:n.1082-200_1082-199del
NM_000770.3:c.1292-200_1292-199del MANE Select	NP_000761.3:n.1292-200_1292-199del
NM_001198853.1:c.1082-200_1082-199del	NP_001185782.1:n.1082-200_1082-199del
NM_001198854.1:c.986-200_986-199del	NP_001185783.1:n.986-200_986-199del
NM_001198855.1:c.1082-200_1082-199del	NP_001185784.1:n.1082-200_1082-199del
XR_945610.1:n.1427-200_1427-199del