Canonical Allele Identifier: CA2249011319
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208880_14208884delinsTAATG , CM000679.2:g.14208880_14208884delinsTAATG GRCh38
NC_000017.10:g.14112197_14112201delinsTAATG , CM000679.1:g.14112197_14112201delinsTAATG GRCh37
NC_000017.9:g.14052922_14052926delinsTAATG NCBI36
NG_008034.1:g.144479_144483delinsTAATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+101_*281+105delinsTAATG ENSP00000499396.1:n.*281+101_*281+105delinsTAATG
ENST00000670279.1:c.929-629_929-625delinsTAATG ENSP00000499450.1:n.929-629_929-625delinsTAATG
XR_933974.1:n.1032-629_1032-625delinsTAATG