Canonical Allele Identifier: CA2037230574
Gene: HOXC9 HGNC NCBI
HOXC6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54000761C= , CM000674.2:g.54000761C= GRCh38
NC_000012.11:g.54394545C= , CM000674.1:g.54394545C= GRCh37
NC_000012.10:g.52680812C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303450.5:c.538+35C= (HOXC9) MANE Select ENSP00000302836.4:n.538+35C=
ENST00000303450.4:c.538+35C= (HOXC9) ENSP00000302836.4:n.538+35C=
ENST00000504315.1:c.-193+9947C= (HOXC6) ENSP00000424124.1:n.-193+9947C=
ENST00000504557.1:n.123-1669C= (HOXC9)
ENST00000508190.1:c.538+35C= (HOXC9) ENSP00000423861.1:n.538+35C=
ENST00000509328.1:c.-73+5745C= (HOXC6) ENSP00000423898.1:n.-73+5745C=
ENST00000513209.1:c.166+14751C= ENSP00000476742.1:n.166+14751C=
NM_006897.1:c.538+35C= (HOXC9) NP_008828.1:n.538+35C=
NM_006897.2:c.538+35C= (HOXC9) NP_008828.1:n.538+35C=
NM_006897.3:c.538+35C= (HOXC9) MANE Select NP_008828.1:n.538+35C=
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