Canonical Allele Identifier: CA1309431469
Gene: HOXD13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093517G= , CM000664.2:g.176093517G= GRCh38
NC_000002.11:g.176958245G= , CM000664.1:g.176958245G= GRCh37
NC_000002.10:g.176666491G= NCBI36
NG_008137.1:g.5714G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.627G= MANE Select ENSP00000376322.3:p.Met209=
ENST00000392539.3:c.627G= ENSP00000376322.3:p.Met209=
NM_000523.3:c.627G= NP_000514.2:p.Met209=
XM_011511068.1:c.725-963G= XP_011509370.1:n.725-963G=
XM_011511068.2:c.725-963G= XP_011509370.1:n.725-963G=
NM_000523.4:c.627G= MANE Select NP_000514.2:p.Met209=
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