Canonical Allele Identifier: CA2619096800
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973898_53973909del , CM000674.2:g.53973898_53973909del GRCh38
NC_000012.11:g.54367682_54367693del , CM000674.1:g.54367682_54367693del GRCh37
NC_000012.10:g.52653949_52653960del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.657_668del (HOXC11) ENSP00000243082.4:p.Glu220_Lys223del
ENST00000546378.1:c.657_668del (HOXC11) MANE Select ENSP00000446680.1:p.Glu220_Lys223del
NM_014212.3:c.657_668del (HOXC11) NP_055027.1:p.Glu220_Lys223del
NR_047517.1:n.59+995_59+1006del (HOTAIR)
NM_014212.4:c.657_668del (HOXC11) MANE Select NP_055027.1:p.Glu220_Lys223del