Canonical Allele Identifier: CA385106013
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973903C>G , CM000674.2:g.53973903C>G GRCh38
NC_000012.11:g.54367687C>G , CM000674.1:g.54367687C>G GRCh37
NC_000012.10:g.52653954C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.662C>G (HOXC11) ENSP00000243082.4:p.Pro221Arg
ENST00000546378.1:c.662C>G (HOXC11) MANE Select ENSP00000446680.1:p.Pro221Arg
NM_014212.3:c.662C>G (HOXC11) NP_055027.1:p.Pro221Arg
NR_047517.1:n.59+995G>C (HOTAIR)
NM_014212.4:c.662C>G (HOXC11) MANE Select NP_055027.1:p.Pro221Arg