Canonical Allele Identifier: CA2249011145
Gene: COX10 HGNC NCBI
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.*1306A= MANE Select ENSP00000261643.3:n.*1306A=
ENST00000664217.1:c.*56-35A= ENSP00000499396.1:n.*56-35A=
ENST00000670279.1:c.929-990A= ENSP00000499450.1:n.929-990A=
ENST00000261643.7:c.*1306A= ENSP00000261643.3:n.*1306A=
NM_001303.3:c.*1306A= NP_001294.2:n.*1306A=
XM_011523658.1:c.*1306A= XP_011521960.1:n.*1306A=
XR_933974.1:n.1032-990A=
NM_001303.4:c.*1306A= MANE Select NP_001294.2:n.*1306A=
Search 100 bp 5'
Search 100 bp 3'