Canonical Allele Identifier: CA2636207218
Gene: COX10 HGNC NCBI

Linked Data

gnomAD v4: 17-14069521-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14069521G>A , CM000679.2:g.14069521G>A GRCh38
NC_000017.10:g.13972838G>A , CM000679.1:g.13972838G>A GRCh37
NC_000017.9:g.13913563G>A NCBI36
NG_008034.1:g.5120G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.-85G>A MANE Select ENSP00000261643.3:n.-85G>A
ENST00000664217.1:c.-85G>A ENSP00000499396.1:n.-85G>A
ENST00000670279.1:c.-85G>A ENSP00000499450.1:n.-85G>A
ENST00000429152.6:c.-85G>A ENSP00000397750.2:n.-85G>A
NM_001303.3:c.-85G>A NP_001294.2:n.-85G>A
XM_005256458.1:c.-85G>A XP_005256515.1:n.-85G>A
XM_011523657.1:c.-85G>A XP_011521959.1:n.-85G>A
XM_011523658.1:c.-536G>A XP_011521960.1:n.-536G>A
XR_933974.1:n.19G>A
XR_933975.1:n.19G>A
NM_001303.4:c.-85G>A MANE Select NP_001294.2:n.-85G>A
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