Canonical Allele Identifier: CA2619103795

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54000729A>G , CM000674.2:g.54000729A>G GRCh38
NC_000012.11:g.54394513A>G , CM000674.1:g.54394513A>G GRCh37
NC_000012.10:g.52680780A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303450.5:c.538+3A>G (HOXC9) MANE Select ENSP00000302836.4:n.538+3A>G
ENST00000303450.4:c.538+3A>G (HOXC9) ENSP00000302836.4:n.538+3A>G
ENST00000504315.1:c.-193+9915A>G (HOXC6) ENSP00000424124.1:n.-193+9915A>G
ENST00000504557.1:n.123-1701A>G (HOXC9)
ENST00000508190.1:c.538+3A>G (HOXC9) ENSP00000423861.1:n.538+3A>G
ENST00000509328.1:c.-73+5713A>G (HOXC6) ENSP00000423898.1:n.-73+5713A>G
ENST00000513209.1:c.166+14719A>G ENSP00000476742.1:n.166+14719A>G
NM_006897.1:c.538+3A>G (HOXC9) NP_008828.1:n.538+3A>G
NM_006897.2:c.538+3A>G (HOXC9) NP_008828.1:n.538+3A>G
NM_006897.3:c.538+3A>G (HOXC9) MANE Select NP_008828.1:n.538+3A>G