Canonical Allele Identifier: CA2249011169
Gene: COX10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208564T= , CM000679.2:g.14208564T= GRCh38
NC_000017.10:g.14111881T= , CM000679.1:g.14111881T= GRCh37
NC_000017.9:g.14052606T= NCBI36
NG_008034.1:g.144163T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.*1351T= MANE Select ENSP00000261643.3:n.*1351T=
ENST00000664217.1:c.*66T= ENSP00000499396.1:n.*66T=
ENST00000670279.1:c.929-945T= ENSP00000499450.1:n.929-945T=
ENST00000261643.7:c.*1351T= ENSP00000261643.3:n.*1351T=
NM_001303.3:c.*1351T= NP_001294.2:n.*1351T=
XM_011523658.1:c.*1351T= XP_011521960.1:n.*1351T=
XR_933974.1:n.1032-945T=
NM_001303.4:c.*1351T= MANE Select NP_001294.2:n.*1351T=
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