Canonical Allele Identifier: CA2575177263

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54000788G>A , CM000674.2:g.54000788G>A GRCh38
NC_000012.11:g.54394572G>A , CM000674.1:g.54394572G>A GRCh37
NC_000012.10:g.52680839G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303450.5:c.538+62G>A (HOXC9) MANE Select ENSP00000302836.4:n.538+62G>A
ENST00000303450.4:c.538+62G>A (HOXC9) ENSP00000302836.4:n.538+62G>A
ENST00000504315.1:c.-193+9974G>A (HOXC6) ENSP00000424124.1:n.-193+9974G>A
ENST00000504557.1:n.123-1642G>A (HOXC9)
ENST00000508190.1:c.538+62G>A (HOXC9) ENSP00000423861.1:n.538+62G>A
ENST00000509328.1:c.-73+5772G>A (HOXC6) ENSP00000423898.1:n.-73+5772G>A
ENST00000513209.1:c.166+14778G>A ENSP00000476742.1:n.166+14778G>A
NM_006897.1:c.538+62G>A (HOXC9) NP_008828.1:n.538+62G>A
NM_006897.2:c.538+62G>A (HOXC9) NP_008828.1:n.538+62G>A
NM_006897.3:c.538+62G>A (HOXC9) MANE Select NP_008828.1:n.538+62G>A