Canonical Allele Identifier: CA2249011222
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208673_14208678delinsAAGAAC , CM000679.2:g.14208673_14208678delinsAAGAAC GRCh38
NC_000017.10:g.14111990_14111995delinsAAGAAC , CM000679.1:g.14111990_14111995delinsAAGAAC GRCh37
NC_000017.9:g.14052715_14052720delinsAAGAAC NCBI36
NG_008034.1:g.144272_144277delinsAAGAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*175_*180delinsAAGAAC ENSP00000499396.1:n.*175_*180delinsAAGAAC
ENST00000670279.1:c.929-836_929-831delinsAAGAAC ENSP00000499450.1:n.929-836_929-831delinsAAGAAC
NM_001303.3:c.*1460_*1465delinsAAGAAC NP_001294.2:n.*1460_*1465delinsAAGAAC
XM_011523658.1:c.*1460_*1465delinsAAGAAC XP_011521960.1:n.*1460_*1465delinsAAGAAC
XR_933974.1:n.1032-836_1032-831delinsAAGAAC