Canonical Allele Identifier: CA2249011195

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14208615_14208616delinsGC , CM000679.2:g.14208615_14208616delinsGC	GRCh38
NC_000017.10:g.14111932_14111933delinsGC , CM000679.1:g.14111932_14111933delinsGC	GRCh37
NC_000017.9:g.14052657_14052658delinsGC	NCBI36
NG_008034.1:g.144214_144215delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.*1402_*1403delinsGC MANE Select	ENSP00000261643.3:n.*1402_*1403delinsGC
ENST00000664217.1:c.*117_*118delinsGC	ENSP00000499396.1:n.*117_*118delinsGC
ENST00000670279.1:c.929-894_929-893delinsGC	ENSP00000499450.1:n.929-894_929-893delinsGC
ENST00000261643.7:c.*1402_*1403delinsGC	ENSP00000261643.3:n.*1402_*1403delinsGC
NM_001303.3:c.*1402_*1403delinsGC	NP_001294.2:n.*1402_*1403delinsGC
XM_011523658.1:c.*1402_*1403delinsGC	XP_011521960.1:n.*1402_*1403delinsGC
XR_933974.1:n.1032-894_1032-893delinsGC
NM_001303.4:c.*1402_*1403delinsGC MANE Select	NP_001294.2:n.*1402_*1403delinsGC