Canonical Allele Identifier: CA595332686

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1224675286
• gnomAD v2: 10-96796762-TG-T
• gnomAD v3: 10-95037005-TG-T
• gnomAD v4: 10-95037005-TG-T
• MyVariant Identifiers: chr10:g.96796763del (hg19) ; chr10:g.95037006del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037008del , CM000672.2:g.95037008del	GRCh38
NC_000010.10:g.96796765del , CM000672.1:g.96796765del	GRCh37
NC_000010.9:g.96786755del	NCBI36
NG_007972.1:g.37492del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*122del MANE Select	ENSP00000360317.3:n.*122del
ENST00000371270.5:c.*122del	ENSP00000360317.3:n.*122del
ENST00000490994.6:c.*1381del	ENSP00000433314.1:n.*1381del
ENST00000525991.5:c.*1170del	ENSP00000433842.1:n.*1170del
ENST00000526814.5:n.1850del
ENST00000527420.5:c.*452del	ENSP00000433191.1:n.*452del
ENST00000527953.5:n.1889del
ENST00000533320.5:n.1829del
ENST00000535898.5:c.*122del	ENSP00000445062.1:n.*122del
ENST00000539050.5:c.*122del	ENSP00000442343.2:n.*122del
ENST00000623108.3:c.*122del	ENSP00000485110.1:n.*122del
NM_000770.3:c.*122del MANE Select	NP_000761.3:n.*122del
NM_001198853.1:c.*122del	NP_001185782.1:n.*122del
NM_001198854.1:c.*122del	NP_001185783.1:n.*122del
NM_001198855.1:c.*122del	NP_001185784.1:n.*122del