Canonical Allele Identifier: CA398248239
Gene: COX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14076889G>C , CM000679.2:g.14076889G>C GRCh38
NC_000017.10:g.13980206G>C , CM000679.1:g.13980206G>C GRCh37
NC_000017.9:g.13920931G>C NCBI36
NG_008034.1:g.12488G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.332G>C MANE Select ENSP00000261643.3:p.Arg111Thr
ENST00000664217.1:c.332G>C ENSP00000499396.1:p.Arg111Thr
ENST00000670279.1:c.332G>C ENSP00000499450.1:p.Arg111Thr
ENST00000261643.7:c.332G>C ENSP00000261643.3:p.Arg111Thr
ENST00000429152.6:c.332G>C ENSP00000397750.2:p.Arg111Thr
ENST00000580561.1:c.177+2433G>C ENSP00000462190.1:n.177+2433G>C
ENST00000581931.5:c.332G>C ENSP00000462512.1:p.Arg111Thr
NM_001303.3:c.332G>C NP_001294.2:p.Arg111Thr
XM_005256458.1:c.332G>C XP_005256515.1:p.Arg111Thr
XM_011523657.1:c.332G>C XP_011521959.1:p.Arg111Thr
XM_011523658.1:c.-120G>C XP_011521960.1:n.-120G>C
XR_933974.1:n.435G>C
XR_933975.1:n.435G>C
NM_001303.4:c.332G>C MANE Select NP_001294.2:p.Arg111Thr