Canonical Allele Identifier: CA1309431490
Gene: HOXD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093572G= , CM000664.2:g.176093572G= GRCh38
NC_000002.11:g.176958300G= , CM000664.1:g.176958300G= GRCh37
NC_000002.10:g.176666546G= NCBI36
NG_008137.1:g.5769G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.682G= MANE Select ENSP00000376322.3:p.Gly228=
ENST00000392539.3:c.682G= ENSP00000376322.3:p.Gly228=
NM_000523.3:c.682G= NP_000514.2:p.Gly228=
XM_011511068.1:c.725-908G= XP_011509370.1:n.725-908G=
XM_011511068.2:c.725-908G= XP_011509370.1:n.725-908G=
NM_000523.4:c.682G= MANE Select NP_000514.2:p.Gly228=