Canonical Allele Identifier: CA1309431453
Gene: HOXD13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093489A= , CM000664.2:g.176093489A= GRCh38
NC_000002.11:g.176958217A= , CM000664.1:g.176958217A= GRCh37
NC_000002.10:g.176666463A= NCBI36
NG_008137.1:g.5686A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.599A= MANE Select ENSP00000376322.3:p.Tyr200=
ENST00000392539.3:c.599A= ENSP00000376322.3:p.Tyr200=
NM_000523.3:c.599A= NP_000514.2:p.Tyr200=
XM_011511068.1:c.725-991A= XP_011509370.1:n.725-991A=
XM_011511068.2:c.725-991A= XP_011509370.1:n.725-991A=
NM_000523.4:c.599A= MANE Select NP_000514.2:p.Tyr200=
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