Canonical Allele Identifier: CA2249011186

Gene: COX10

Linked Data

• dbSNP Id: rs1906779074

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14208604_14208605insGCTGCT , CM000679.2:g.14208604_14208605insGCTGCT	GRCh38
NC_000017.10:g.14111921_14111922insGCTGCT , CM000679.1:g.14111921_14111922insGCTGCT	GRCh37
NC_000017.9:g.14052646_14052647insGCTGCT	NCBI36
NG_008034.1:g.144203_144204insGCTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.*1391_*1392insGCTGCT MANE Select	ENSP00000261643.3:n.*1391_*1392insGCTGCT
ENST00000664217.1:c.*106_*107insGCTGCT	ENSP00000499396.1:n.*106_*107insGCTGCT
ENST00000670279.1:c.929-905_929-904insGCTGCT	ENSP00000499450.1:n.929-905_929-904insGCTGCT
ENST00000261643.7:c.*1391_*1392insGCTGCT	ENSP00000261643.3:n.*1391_*1392insGCTGCT
NM_001303.3:c.*1391_*1392insGCTGCT	NP_001294.2:n.*1391_*1392insGCTGCT
XM_011523658.1:c.*1391_*1392insGCTGCT	XP_011521960.1:n.*1391_*1392insGCTGCT
XR_933974.1:n.1032-905_1032-904insGCTGCT
NM_001303.4:c.*1391_*1392insGCTGCT MANE Select	NP_001294.2:n.*1391_*1392insGCTGCT