Canonical Allele Identifier: CA2577165631
Gene: HOXD13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093678del , CM000664.2:g.176093678del GRCh38
NC_000002.11:g.176958406del , CM000664.1:g.176958406del GRCh37
NC_000002.10:g.176666652del NCBI36
NG_008137.1:g.5875del

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.781+7del MANE Select ENSP00000376322.3:n.781+7del
ENST00000392539.3:c.781+7del ENSP00000376322.3:n.781+7del
NM_000523.3:c.781+7del NP_000514.2:n.781+7del
XM_011511068.1:c.725-802del XP_011509370.1:n.725-802del
XM_011511068.2:c.725-802del XP_011509370.1:n.725-802del
NM_000523.4:c.781+7del MANE Select NP_000514.2:n.781+7del