Canonical Allele Identifier: CA1139770130
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973801_53973802insAGGGGGGGGGGGGGGG , CM000674.2:g.53973801_53973802insAGGGGGGGGGGGGGGG GRCh38
NC_000012.11:g.54367585_54367586insAGGGGGGGGGGGGGGG , CM000674.1:g.54367585_54367586insAGGGGGGGGGGGGGGG GRCh37
NC_000012.10:g.52653852_52653853insAGGGGGGGGGGGGGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.560_561insAGGGGGGGGGGGGGGG (HOXC11) ENSP00000243082.4:p.Leu189GlyfsTer11
ENST00000546378.1:c.560_561insAGGGGGGGGGGGGGGG (HOXC11) MANE Select ENSP00000446680.1:p.Leu189GlyfsTer11
NM_014212.3:c.560_561insAGGGGGGGGGGGGGGG (HOXC11) NP_055027.1:p.Leu189GlyfsTer11
NR_047517.1:n.59+1096_59+1097insCCCCCCCCCCCCCCCT (HOTAIR)
NM_014212.4:c.560_561insAGGGGGGGGGGGGGGG (HOXC11) MANE Select NP_055027.1:p.Leu189GlyfsTer11