Canonical Allele Identifier: CA2808557400
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208636A>T , CM000679.2:g.14208636A>T GRCh38
NC_000017.10:g.14111953A>T , CM000679.1:g.14111953A>T GRCh37
NC_000017.9:g.14052678A>T NCBI36
NG_008034.1:g.144235A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.*1423A>T MANE Select ENSP00000261643.3:n.*1423A>T
ENST00000664217.1:c.*138A>T ENSP00000499396.1:n.*138A>T
ENST00000670279.1:c.929-873A>T ENSP00000499450.1:n.929-873A>T
ENST00000261643.7:c.*1423A>T ENSP00000261643.3:n.*1423A>T
NM_001303.3:c.*1423A>T NP_001294.2:n.*1423A>T
XM_011523658.1:c.*1423A>T XP_011521960.1:n.*1423A>T
XR_933974.1:n.1032-873A>T
NM_001303.4:c.*1423A>T MANE Select NP_001294.2:n.*1423A>T