Canonical Allele Identifier: CA2249011146

Gene: COX10

Linked Data

• dbSNP Id: rs1906776527

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14208519A>G , CM000679.2:g.14208519A>G	GRCh38
NC_000017.10:g.14111836A>G , CM000679.1:g.14111836A>G	GRCh37
NC_000017.9:g.14052561A>G	NCBI36
NG_008034.1:g.144118A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.*1306A>G MANE Select	ENSP00000261643.3:n.*1306A>G
ENST00000664217.1:c.*56-35A>G	ENSP00000499396.1:n.*56-35A>G
ENST00000670279.1:c.929-990A>G	ENSP00000499450.1:n.929-990A>G
ENST00000261643.7:c.*1306A>G	ENSP00000261643.3:n.*1306A>G
NM_001303.3:c.*1306A>G	NP_001294.2:n.*1306A>G
XM_011523658.1:c.*1306A>G	XP_011521960.1:n.*1306A>G
XR_933974.1:n.1032-990A>G
NM_001303.4:c.*1306A>G MANE Select	NP_001294.2:n.*1306A>G