Canonical Allele Identifier: CA1309431484
Gene: HOXD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093558A= , CM000664.2:g.176093558A= GRCh38
NC_000002.11:g.176958286A= , CM000664.1:g.176958286A= GRCh37
NC_000002.10:g.176666532A= NCBI36
NG_008137.1:g.5755A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.668A= MANE Select ENSP00000376322.3:p.Tyr223=
ENST00000392539.3:c.668A= ENSP00000376322.3:p.Tyr223=
NM_000523.3:c.668A= NP_000514.2:p.Tyr223=
XM_011511068.1:c.725-922A= XP_011509370.1:n.725-922A=
XM_011511068.2:c.725-922A= XP_011509370.1:n.725-922A=
NM_000523.4:c.668A= MANE Select NP_000514.2:p.Tyr223=