Canonical Allele Identifier: CA2636210041
Gene: COX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208554G>T , CM000679.2:g.14208554G>T GRCh38
NC_000017.10:g.14111871G>T , CM000679.1:g.14111871G>T GRCh37
NC_000017.9:g.14052596G>T NCBI36
NG_008034.1:g.144153G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.*1341G>T MANE Select ENSP00000261643.3:n.*1341G>T
ENST00000664217.1:c.*56G>T ENSP00000499396.1:n.*56G>T
ENST00000670279.1:c.929-955G>T ENSP00000499450.1:n.929-955G>T
ENST00000261643.7:c.*1341G>T ENSP00000261643.3:n.*1341G>T
NM_001303.3:c.*1341G>T NP_001294.2:n.*1341G>T
XM_011523658.1:c.*1341G>T XP_011521960.1:n.*1341G>T
XR_933974.1:n.1032-955G>T
NM_001303.4:c.*1341G>T MANE Select NP_001294.2:n.*1341G>T