Canonical Allele Identifier: CA2619104274

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54000814C>A , CM000674.2:g.54000814C>A GRCh38
NC_000012.11:g.54394598C>A , CM000674.1:g.54394598C>A GRCh37
NC_000012.10:g.52680865C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303450.5:c.538+88C>A (HOXC9) MANE Select ENSP00000302836.4:n.538+88C>A
ENST00000303450.4:c.538+88C>A (HOXC9) ENSP00000302836.4:n.538+88C>A
ENST00000504315.1:c.-193+10000C>A (HOXC6) ENSP00000424124.1:n.-193+10000C>A
ENST00000504557.1:n.123-1616C>A (HOXC9)
ENST00000508190.1:c.538+88C>A (HOXC9) ENSP00000423861.1:n.538+88C>A
ENST00000509328.1:c.-73+5798C>A (HOXC6) ENSP00000423898.1:n.-73+5798C>A
ENST00000513209.1:c.166+14804C>A ENSP00000476742.1:n.166+14804C>A
NM_006897.1:c.538+88C>A (HOXC9) NP_008828.1:n.538+88C>A
NM_006897.2:c.538+88C>A (HOXC9) NP_008828.1:n.538+88C>A
NM_006897.3:c.538+88C>A (HOXC9) MANE Select NP_008828.1:n.538+88C>A