Canonical Allele Identifier: CA2249011175
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208587C= , CM000679.2:g.14208587C= GRCh38
NC_000017.10:g.14111904C= , CM000679.1:g.14111904C= GRCh37
NC_000017.9:g.14052629C= NCBI36
NG_008034.1:g.144186C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.*1374C= MANE Select ENSP00000261643.3:n.*1374C=
ENST00000664217.1:c.*89C= ENSP00000499396.1:n.*89C=
ENST00000670279.1:c.929-922C= ENSP00000499450.1:n.929-922C=
ENST00000261643.7:c.*1374C= ENSP00000261643.3:n.*1374C=
NM_001303.3:c.*1374C= NP_001294.2:n.*1374C=
XM_011523658.1:c.*1374C= XP_011521960.1:n.*1374C=
XR_933974.1:n.1032-922C=
NM_001303.4:c.*1374C= MANE Select NP_001294.2:n.*1374C=