Canonical Allele Identifier: CA1309445292
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1689813062
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118903C>A , CM000664.2:g.176118903C>A GRCh38
NC_000002.11:g.176983631C>A , CM000664.1:g.176983631C>A GRCh37
NC_000002.10:g.176691877C>A NCBI36
NG_008133.2:g.12140C>A , LRG_246:g.12140C>A
NG_009225.1:g.1219C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.746-51C>A MANE Select ENSP00000249501.4:n.746-51C>A
ENST00000249501.4:c.746-51C>A ENSP00000249501.4:n.746-51C>A
ENST00000490088.2:n.570-51C>A
ENST00000549469.1:n.617-51C>A
NM_002148.3:c.746-51C>A , LRG_246t1:c.746-51C>A NP_002139.2:n.746-51C>A
NM_002148.4:c.746-51C>A MANE Select NP_002139.2:n.746-51C>A
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