Canonical Allele Identifier: CA385105878
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

dbSNP Id: rs994008655

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973875G>T , CM000674.2:g.53973875G>T GRCh38
NC_000012.11:g.54367659G>T , CM000674.1:g.54367659G>T GRCh37
NC_000012.10:g.52653926G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.634G>T (HOXC11) ENSP00000243082.4:p.Gly212Cys
ENST00000546378.1:c.634G>T (HOXC11) MANE Select ENSP00000446680.1:p.Gly212Cys
NM_014212.3:c.634G>T (HOXC11) NP_055027.1:p.Gly212Cys
NR_047517.1:n.59+1023C>A (HOTAIR)
NM_014212.4:c.634G>T (HOXC11) MANE Select NP_055027.1:p.Gly212Cys