Canonical Allele Identifier: CA2249011234
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208706_14208709delinsAATC , CM000679.2:g.14208706_14208709delinsAATC GRCh38
NC_000017.10:g.14112023_14112026delinsAATC , CM000679.1:g.14112023_14112026delinsAATC GRCh37
NC_000017.9:g.14052748_14052751delinsAATC NCBI36
NG_008034.1:g.144305_144308delinsAATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*208_*211delinsAATC ENSP00000499396.1:n.*208_*211delinsAATC
ENST00000670279.1:c.929-803_929-800delinsAATC ENSP00000499450.1:n.929-803_929-800delinsAATC
XR_933974.1:n.1032-803_1032-800delinsAATC