Canonical Allele Identifier: CA625321057
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs879195393
gnomAD v2: 17-13972832-A-AG
gnomAD v3: 17-14069515-A-AG
gnomAD v4: 17-14069515-A-AG
MyVariant Identifiers: chr17:g.13972832_13972833insG (hg19) chr17:g.14069515_14069516insG (hg38)
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Genomic Alleles

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

Transcript Alleles

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