Canonical Allele Identifier: CA1929375689
Gene: CYP2C8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95037437A= , CM000672.2:g.95037437A= GRCh38
NC_000010.10:g.96797194A= , CM000672.1:g.96797194A= GRCh37
NC_000010.9:g.96787184A= NCBI36
NG_007972.1:g.37061T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371270.6:c.1292-128T= MANE Select ENSP00000360317.3:n.1292-128T=
ENST00000371270.5:c.1292-128T= ENSP00000360317.3:n.1292-128T=
ENST00000490994.6:c.*1078-128T= ENSP00000433314.1:n.*1078-128T=
ENST00000525991.5:c.*867-128T= ENSP00000433842.1:n.*867-128T=
ENST00000526814.5:n.1547-128T=
ENST00000527420.5:c.*149-128T= ENSP00000433191.1:n.*149-128T=
ENST00000527953.5:n.1586-128T=
ENST00000531714.1:n.480-128T=
ENST00000533320.5:n.1526-128T=
ENST00000535898.5:c.986-128T= ENSP00000445062.1:n.986-128T=
ENST00000539050.5:c.1082-128T= ENSP00000442343.2:n.1082-128T=
ENST00000623108.3:c.1082-128T= ENSP00000485110.1:n.1082-128T=
NM_000770.3:c.1292-128T= MANE Select NP_000761.3:n.1292-128T=
NM_001198853.1:c.1082-128T= NP_001185782.1:n.1082-128T=
NM_001198854.1:c.986-128T= NP_001185783.1:n.986-128T=
NM_001198855.1:c.1082-128T= NP_001185784.1:n.1082-128T=
XR_945610.1:n.1427-128T=