Canonical Allele Identifier: CA1929357642
Gene: CYP2C8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95038901T= , CM000672.2:g.95038901T= GRCh38
NC_000010.10:g.96798658T= , CM000672.1:g.96798658T= GRCh37
NC_000010.9:g.96788648T= NCBI36
NG_007972.1:g.35597A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371270.6:c.1287A= MANE Select ENSP00000360317.3:p.Ser429=
ENST00000371270.5:c.1287A= ENSP00000360317.3:p.Ser429=
ENST00000490994.6:c.*1073A= ENSP00000433314.1:n.*1073A=
ENST00000525991.5:c.*862A= ENSP00000433842.1:n.*862A=
ENST00000526814.5:n.1542A=
ENST00000527420.5:c.*144A= ENSP00000433191.1:n.*144A=
ENST00000527953.5:n.1581A=
ENST00000531714.1:n.475A=
ENST00000533320.5:n.1521A=
ENST00000535898.5:c.981A= ENSP00000445062.1:p.Ser327=
ENST00000539050.5:c.1077A= ENSP00000442343.2:p.Ser359=
ENST00000623108.3:c.1077A= ENSP00000485110.1:p.Ser359=
NM_000770.3:c.1287A= MANE Select NP_000761.3:p.Ser429=
NM_001198853.1:c.1077A= NP_001185782.1:p.Ser359=
NM_001198854.1:c.981A= NP_001185783.1:p.Ser327=
NM_001198855.1:c.1077A= NP_001185784.1:p.Ser359=
XR_945610.1:n.1422A=