Canonical Allele Identifier: CA1309445533
Gene: HOXD10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119428C= , CM000664.2:g.176119428C= GRCh38
NC_000002.11:g.176984156C= , CM000664.1:g.176984156C= GRCh37
NC_000002.10:g.176692402C= NCBI36
NG_008133.2:g.12665C= , LRG_246:g.12665C=
NG_009225.1:g.1744C=

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.*197C= MANE Select ENSP00000249501.4:n.*197C=
ENST00000249501.4:c.*197C= ENSP00000249501.4:n.*197C=
NM_002148.3:c.*197C= , LRG_246t1:c.*197C= NP_002139.2:n.*197C=
NM_002148.4:c.*197C= MANE Select NP_002139.2:n.*197C=
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