Canonical Allele Identifier: CA2249011197

Gene: COX10

Linked Data

• dbSNP Id: rs1906779748

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14208617del , CM000679.2:g.14208617del	GRCh38
NC_000017.10:g.14111934del , CM000679.1:g.14111934del	GRCh37
NC_000017.9:g.14052659del	NCBI36
NG_008034.1:g.144216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.*1404del MANE Select	ENSP00000261643.3:n.*1404del
ENST00000664217.1:c.*119del	ENSP00000499396.1:n.*119del
ENST00000670279.1:c.929-892del	ENSP00000499450.1:n.929-892del
ENST00000261643.7:c.*1404del	ENSP00000261643.3:n.*1404del
NM_001303.3:c.*1404del	NP_001294.2:n.*1404del
XM_011523658.1:c.*1404del	XP_011521960.1:n.*1404del
XR_933974.1:n.1032-892del
NM_001303.4:c.*1404del MANE Select	NP_001294.2:n.*1404del