Canonical Allele Identifier: CA2249011190
Gene: COX10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208612A= , CM000679.2:g.14208612A= GRCh38
NC_000017.10:g.14111929A= , CM000679.1:g.14111929A= GRCh37
NC_000017.9:g.14052654A= NCBI36
NG_008034.1:g.144211A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.*1399A= MANE Select ENSP00000261643.3:n.*1399A=
ENST00000664217.1:c.*114A= ENSP00000499396.1:n.*114A=
ENST00000670279.1:c.929-897A= ENSP00000499450.1:n.929-897A=
ENST00000261643.7:c.*1399A= ENSP00000261643.3:n.*1399A=
NM_001303.3:c.*1399A= NP_001294.2:n.*1399A=
XM_011523658.1:c.*1399A= XP_011521960.1:n.*1399A=
XR_933974.1:n.1032-897A=
NM_001303.4:c.*1399A= MANE Select NP_001294.2:n.*1399A=
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