Canonical Allele Identifier: CA1309431437
Gene: HOXD13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093459T= , CM000664.2:g.176093459T= GRCh38
NC_000002.11:g.176958187T= , CM000664.1:g.176958187T= GRCh37
NC_000002.10:g.176666433T= NCBI36
NG_008137.1:g.5656T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.569T= MANE Select ENSP00000376322.3:p.Val190=
ENST00000392539.3:c.569T= ENSP00000376322.3:p.Val190=
NM_000523.3:c.569T= NP_000514.2:p.Val190=
XM_011511068.1:c.725-1021T= XP_011509370.1:n.725-1021T=
XM_011511068.2:c.725-1021T= XP_011509370.1:n.725-1021T=
NM_000523.4:c.569T= MANE Select NP_000514.2:p.Val190=
Search 100 bp 5'
Search 100 bp 3'