Canonical Allele Identifier: CA2249011218
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208671_14208672delinsAC , CM000679.2:g.14208671_14208672delinsAC GRCh38
NC_000017.10:g.14111988_14111989delinsAC , CM000679.1:g.14111988_14111989delinsAC GRCh37
NC_000017.9:g.14052713_14052714delinsAC NCBI36
NG_008034.1:g.144270_144271delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.*1458_*1459delinsAC MANE Select ENSP00000261643.3:n.*1458_*1459delinsAC
ENST00000664217.1:c.*173_*174delinsAC ENSP00000499396.1:n.*173_*174delinsAC
ENST00000670279.1:c.929-838_929-837delinsAC ENSP00000499450.1:n.929-838_929-837delinsAC
ENST00000261643.7:c.*1458_*1459delinsAC ENSP00000261643.3:n.*1458_*1459delinsAC
NM_001303.3:c.*1458_*1459delinsAC NP_001294.2:n.*1458_*1459delinsAC
XM_011523658.1:c.*1458_*1459delinsAC XP_011521960.1:n.*1458_*1459delinsAC
XR_933974.1:n.1032-838_1032-837delinsAC
NM_001303.4:c.*1458_*1459delinsAC MANE Select NP_001294.2:n.*1458_*1459delinsAC