Canonical Allele Identifier: CA385104752
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

dbSNP Id: rs748624439

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973674A>C , CM000674.2:g.53973674A>C GRCh38
NC_000012.11:g.54367458A>C , CM000674.1:g.54367458A>C GRCh37
NC_000012.10:g.52653725A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.433A>C (HOXC11) ENSP00000243082.4:p.Ser145Arg
ENST00000546378.1:c.433A>C (HOXC11) MANE Select ENSP00000446680.1:p.Ser145Arg
NM_014212.3:c.433A>C (HOXC11) NP_055027.1:p.Ser145Arg
NR_047517.1:n.59+1224T>G (HOTAIR)
NM_014212.4:c.433A>C (HOXC11) MANE Select NP_055027.1:p.Ser145Arg