Canonical Allele Identifier: CA1309445323
Gene: HOXD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118961C= , CM000664.2:g.176118961C= GRCh38
NC_000002.11:g.176983689C= , CM000664.1:g.176983689C= GRCh37
NC_000002.10:g.176691935C= NCBI36
NG_008133.2:g.12198C= , LRG_246:g.12198C=
NG_009225.1:g.1277C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.753C= MANE Select ENSP00000249501.4:p.Ile251=
ENST00000249501.4:c.753C= ENSP00000249501.4:p.Ile251=
ENST00000490088.2:n.577C=
ENST00000549469.1:n.624C=
NM_002148.3:c.753C= , LRG_246t1:c.753C= NP_002139.2:p.Ile251=
NM_002148.4:c.753C= MANE Select NP_002139.2:p.Ile251=