Canonical Allele Identifier: CA2249011281
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208789_14208790delinsAG , CM000679.2:g.14208789_14208790delinsAG GRCh38
NC_000017.10:g.14112106_14112107delinsAG , CM000679.1:g.14112106_14112107delinsAG GRCh37
NC_000017.9:g.14052831_14052832delinsAG NCBI36
NG_008034.1:g.144388_144389delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+10_*281+11delinsAG ENSP00000499396.1:n.*281+10_*281+11delinsAG
ENST00000670279.1:c.929-720_929-719delinsAG ENSP00000499450.1:n.929-720_929-719delinsAG
XR_933974.1:n.1032-720_1032-719delinsAG