Canonical Allele Identifier: CA2249011306
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208841_14208844delinsGTAA , CM000679.2:g.14208841_14208844delinsGTAA GRCh38
NC_000017.10:g.14112158_14112161delinsGTAA , CM000679.1:g.14112158_14112161delinsGTAA GRCh37
NC_000017.9:g.14052883_14052886delinsGTAA NCBI36
NG_008034.1:g.144440_144443delinsGTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+62_*281+65delinsGTAA ENSP00000499396.1:n.*281+62_*281+65delinsGTAA
ENST00000670279.1:c.929-668_929-665delinsGTAA ENSP00000499450.1:n.929-668_929-665delinsGTAA
XR_933974.1:n.1032-668_1032-665delinsGTAA