Canonical Allele Identifier: CA385116254
Gene: HOXC9 HGNC NCBI
HOXC6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.54394498G>C (hg19) chr12:g.54000714G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54000714G>C , CM000674.2:g.54000714G>C GRCh38
NC_000012.11:g.54394498G>C , CM000674.1:g.54394498G>C GRCh37
NC_000012.10:g.52680765G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000303450.5:c.526G>C (HOXC9) MANE Select ENSP00000302836.4:p.Asp176His
ENST00000303450.4:c.526G>C (HOXC9) ENSP00000302836.4:p.Asp176His
ENST00000504315.1:c.-193+9900G>C (HOXC6) ENSP00000424124.1:n.-193+9900G>C
ENST00000504557.1:n.123-1716G>C (HOXC9)
ENST00000508190.1:c.526G>C (HOXC9) ENSP00000423861.1:p.Asp176His
ENST00000509328.1:c.-73+5698G>C (HOXC6) ENSP00000423898.1:n.-73+5698G>C
ENST00000513209.1:c.166+14704G>C ENSP00000476742.1:n.166+14704G>C
NM_006897.1:c.526G>C (HOXC9) NP_008828.1:p.Asp176His
NM_006897.2:c.526G>C (HOXC9) NP_008828.1:p.Asp176His
NM_006897.3:c.526G>C (HOXC9) MANE Select NP_008828.1:p.Asp176His
Search 100 bp 5'
Search 100 bp 3'