Canonical Allele Identifier: CA761094535
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1223278840
MyVariant Identifiers: chr2:g.176983610_176983625del (hg19) chr2:g.176118882_176118897del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118883_176118898del , CM000664.2:g.176118883_176118898del GRCh38
NC_000002.11:g.176983611_176983626del , CM000664.1:g.176983611_176983626del GRCh37
NC_000002.10:g.176691857_176691872del NCBI36
NG_008133.2:g.12120_12135del , LRG_246:g.12120_12135del
NG_009225.1:g.1199_1214del

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.746-71_746-56del MANE Select ENSP00000249501.4:n.746-71_746-56del
ENST00000249501.4:c.746-71_746-56del ENSP00000249501.4:n.746-71_746-56del
ENST00000490088.2:n.570-71_570-56del
ENST00000549469.1:n.617-71_617-56del
NM_002148.3:c.746-71_746-56del , LRG_246t1:c.746-71_746-56del NP_002139.2:n.746-71_746-56del
NM_002148.4:c.746-71_746-56del MANE Select NP_002139.2:n.746-71_746-56del
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Search 100 bp 3'