Canonical Allele Identifier: CA385105664
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973836G>A , CM000674.2:g.53973836G>A GRCh38
NC_000012.11:g.54367620G>A , CM000674.1:g.54367620G>A GRCh37
NC_000012.10:g.52653887G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.595G>A (HOXC11) ENSP00000243082.4:p.Ala199Thr
ENST00000546378.1:c.595G>A (HOXC11) MANE Select ENSP00000446680.1:p.Ala199Thr
NM_014212.3:c.595G>A (HOXC11) NP_055027.1:p.Ala199Thr
NR_047517.1:n.59+1062C>T (HOTAIR)
NM_014212.4:c.595G>A (HOXC11) MANE Select NP_055027.1:p.Ala199Thr