Canonical Allele Identifier: CA2573134021
Community Standard Title: NM_000523.4(HOXD13):c.186_212dup (p.Ala63_Ala71dup)
Gene: HOXD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093076_176093102dup , CM000664.2:g.176093076_176093102dup GRCh38
NC_000002.11:g.176957804_176957830dup , CM000664.1:g.176957804_176957830dup GRCh37
NC_000002.10:g.176666050_176666076dup NCBI36
NG_008137.1:g.5273_5299dup

Transcript Alleles

HGVS Amino-acid Change
NM_000523.4:c.186_212dup MANE Select NP_000514.2:p.Ala71_Ser72insAlaAlaAlaAlaAlaAlaAlaAlaAla
ENST00000392539.4:c.186_212dup MANE Select ENSP00000376322.3:p.Ala71_Ser72insAlaAlaAlaAlaAlaAlaAlaAlaAla...
NM_000523.3:c.186_212dup NP_000514.2:p.Ala71_Ser72insAlaAlaAlaAlaAlaAlaAlaAlaAla
ENST00000392539.3:c.186_212dup ENSP00000376322.3:p.Ala71_Ser72insAlaAlaAlaAlaAlaAlaAlaAlaAla...
XM_011511068.1:c.725-1404_725-1378dup XP_011509370.1:n.725-1404_725-1378dup
XM_011511068.2:c.725-1404_725-1378dup XP_011509370.1:n.725-1404_725-1378dup