Canonical Allele Identifier: CA1309431472
Gene: HOXD13 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093528T= , CM000664.2:g.176093528T= GRCh38
NC_000002.11:g.176958256T= , CM000664.1:g.176958256T= GRCh37
NC_000002.10:g.176666502T= NCBI36
NG_008137.1:g.5725T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.638T= MANE Select ENSP00000376322.3:p.Phe213=
ENST00000392539.3:c.638T= ENSP00000376322.3:p.Phe213=
NM_000523.3:c.638T= NP_000514.2:p.Phe213=
XM_011511068.1:c.725-952T= XP_011509370.1:n.725-952T=
XM_011511068.2:c.725-952T= XP_011509370.1:n.725-952T=
NM_000523.4:c.638T= MANE Select NP_000514.2:p.Phe213=
Search 100 bp 5'
Search 100 bp 3'