Canonical Allele Identifier: CA377677382
Gene: CYP2C8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95037205T>C , CM000672.2:g.95037205T>C GRCh38
NC_000010.10:g.96796962T>C , CM000672.1:g.96796962T>C GRCh37
NC_000010.9:g.96786952T>C NCBI36
NG_007972.1:g.37293A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371270.6:c.1396A>G MANE Select ENSP00000360317.3:p.Asn466Asp
ENST00000371270.5:c.1396A>G ENSP00000360317.3:p.Asn466Asp
ENST00000490994.6:c.*1182A>G ENSP00000433314.1:n.*1182A>G
ENST00000525991.5:c.*971A>G ENSP00000433842.1:n.*971A>G
ENST00000526814.5:n.1651A>G
ENST00000527420.5:c.*253A>G ENSP00000433191.1:n.*253A>G
ENST00000527953.5:n.1690A>G
ENST00000531714.1:n.584A>G
ENST00000533320.5:n.1630A>G
ENST00000535898.5:c.1090A>G ENSP00000445062.1:p.Asn364Asp
ENST00000539050.5:c.1186A>G ENSP00000442343.2:p.Asn396Asp
ENST00000623108.3:c.1186A>G ENSP00000485110.1:p.Asn396Asp
NM_000770.3:c.1396A>G MANE Select NP_000761.3:p.Asn466Asp
NM_001198853.1:c.1186A>G NP_001185782.1:p.Asn396Asp
NM_001198854.1:c.1090A>G NP_001185783.1:p.Asn364Asp
NM_001198855.1:c.1186A>G NP_001185784.1:p.Asn396Asp
XR_945610.1:n.1531A>G