Canonical Allele Identifier: CA2249011168
Gene: COX10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208563G= , CM000679.2:g.14208563G= GRCh38
NC_000017.10:g.14111880G= , CM000679.1:g.14111880G= GRCh37
NC_000017.9:g.14052605G= NCBI36
NG_008034.1:g.144162G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.*1350G= MANE Select ENSP00000261643.3:n.*1350G=
ENST00000664217.1:c.*65G= ENSP00000499396.1:n.*65G=
ENST00000670279.1:c.929-946G= ENSP00000499450.1:n.929-946G=
ENST00000261643.7:c.*1350G= ENSP00000261643.3:n.*1350G=
NM_001303.3:c.*1350G= NP_001294.2:n.*1350G=
XM_011523658.1:c.*1350G= XP_011521960.1:n.*1350G=
XR_933974.1:n.1032-946G=
NM_001303.4:c.*1350G= MANE Select NP_001294.2:n.*1350G=
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