Canonical Allele Identifier: CA385105935
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973887T>C , CM000674.2:g.53973887T>C GRCh38
NC_000012.11:g.54367671T>C , CM000674.1:g.54367671T>C GRCh37
NC_000012.10:g.52653938T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.646T>C (HOXC11) ENSP00000243082.4:p.Ser216Pro
ENST00000546378.1:c.646T>C (HOXC11) MANE Select ENSP00000446680.1:p.Ser216Pro
NM_014212.3:c.646T>C (HOXC11) NP_055027.1:p.Ser216Pro
NR_047517.1:n.59+1011A>G (HOTAIR)
NM_014212.4:c.646T>C (HOXC11) MANE Select NP_055027.1:p.Ser216Pro