Canonical Allele Identifier: CA595333047

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1272585922
• gnomAD v2: 10-96797359-CTTTA-C
• gnomAD v3: 10-95037602-CTTTA-C
• gnomAD v4: 10-95037602-CTTTA-C
• MyVariant Identifiers: chr10:g.96797360_96797363del (hg19) ; chr10:g.95037603_95037606del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037609_95037612del , CM000672.2:g.95037609_95037612del	GRCh38
NC_000010.10:g.96797366_96797369del , CM000672.1:g.96797366_96797369del	GRCh37
NC_000010.9:g.96787356_96787359del	NCBI36
NG_007972.1:g.36892_36895del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-297_1292-294del MANE Select	ENSP00000360317.3:n.1292-297_1292-294del
ENST00000371270.5:c.1292-297_1292-294del	ENSP00000360317.3:n.1292-297_1292-294del
ENST00000490994.6:c.*1078-297_*1078-294del	ENSP00000433314.1:n.*1078-297_*1078-294del
ENST00000525991.5:c.*867-297_*867-294del	ENSP00000433842.1:n.*867-297_*867-294del
ENST00000526814.5:n.1547-297_1547-294del
ENST00000527420.5:c.*149-297_*149-294del	ENSP00000433191.1:n.*149-297_*149-294del
ENST00000527953.5:n.1586-297_1586-294del
ENST00000531714.1:n.480-297_480-294del
ENST00000533320.5:n.1526-297_1526-294del
ENST00000535898.5:c.986-297_986-294del	ENSP00000445062.1:n.986-297_986-294del
ENST00000539050.5:c.1082-297_1082-294del	ENSP00000442343.2:n.1082-297_1082-294del
ENST00000623108.3:c.1082-297_1082-294del	ENSP00000485110.1:n.1082-297_1082-294del
NM_000770.3:c.1292-297_1292-294del MANE Select	NP_000761.3:n.1292-297_1292-294del
NM_001198853.1:c.1082-297_1082-294del	NP_001185782.1:n.1082-297_1082-294del
NM_001198854.1:c.986-297_986-294del	NP_001185783.1:n.986-297_986-294del
NM_001198855.1:c.1082-297_1082-294del	NP_001185784.1:n.1082-297_1082-294del
XR_945610.1:n.1427-297_1427-294del