Canonical Allele Identifier: CA1309445410
Gene: HOXD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119186A= , CM000664.2:g.176119186A= GRCh38
NC_000002.11:g.176983914A= , CM000664.1:g.176983914A= GRCh37
NC_000002.10:g.176692160A= NCBI36
NG_008133.2:g.12423A= , LRG_246:g.12423A=
NG_009225.1:g.1502A=

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.978A= MANE Select ENSP00000249501.4:p.Arg326=
ENST00000249501.4:c.978A= ENSP00000249501.4:p.Arg326=
ENST00000490088.2:n.802A=
ENST00000549469.1:n.849A=
NM_002148.3:c.978A= , LRG_246t1:c.978A= NP_002139.2:p.Arg326=
NM_002148.4:c.978A= MANE Select NP_002139.2:p.Arg326=