Canonical Allele Identifier: CA1309445332
Gene: HOXD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118983A= , CM000664.2:g.176118983A= GRCh38
NC_000002.11:g.176983711A= , CM000664.1:g.176983711A= GRCh37
NC_000002.10:g.176691957A= NCBI36
NG_008133.2:g.12220A= , LRG_246:g.12220A=
NG_009225.1:g.1299A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.775A= MANE Select ENSP00000249501.4:p.Asn259=
ENST00000249501.4:c.775A= ENSP00000249501.4:p.Asn259=
ENST00000490088.2:n.599A=
ENST00000549469.1:n.646A=
NM_002148.3:c.775A= , LRG_246t1:c.775A= NP_002139.2:p.Asn259=
NM_002148.4:c.775A= MANE Select NP_002139.2:p.Asn259=