Canonical Allele Identifier: CA349370767
Gene: HOXD10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119188A>G , CM000664.2:g.176119188A>G GRCh38
NC_000002.11:g.176983916A>G , CM000664.1:g.176983916A>G GRCh37
NC_000002.10:g.176692162A>G NCBI36
NG_008133.2:g.12425A>G , LRG_246:g.12425A>G
NG_009225.1:g.1504A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.980A>G MANE Select ENSP00000249501.4:p.Glu327Gly
ENST00000249501.4:c.980A>G ENSP00000249501.4:p.Glu327Gly
ENST00000490088.2:n.804A>G
ENST00000549469.1:n.851A>G
NM_002148.3:c.980A>G , LRG_246t1:c.980A>G NP_002139.2:p.Glu327Gly
NM_002148.4:c.980A>G MANE Select NP_002139.2:p.Glu327Gly