Canonical Allele Identifier: CA2619096600
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973800_53973801insGGGGGGGGGGGGGGGGGGGGG , CM000674.2:g.53973800_53973801insGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000012.11:g.54367584_54367585insGGGGGGGGGGGGGGGGGGGGG , CM000674.1:g.54367584_54367585insGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000012.10:g.52653851_52653852insGGGGGGGGGGGGGGGGGGGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.559_560insGGGGGGGGGGGGGGGGGGGGG (HOXC11) ENSP00000243082.4:p.Ser187delinsTrpGlyGlyGlyGlyGlyGlyAla
ENST00000546378.1:c.559_560insGGGGGGGGGGGGGGGGGGGGG (HOXC11) MANE Select ENSP00000446680.1:p.Ser187delinsTrpGlyGlyGlyGlyGlyGlyAla
NM_014212.3:c.559_560insGGGGGGGGGGGGGGGGGGGGG (HOXC11) NP_055027.1:p.Ser187delinsTrpGlyGlyGlyGlyGlyGlyAla
NR_047517.1:n.59+1097_59+1098insCCCCCCCCCCCCCCCCCCCCC (HOTAIR)
NM_014212.4:c.559_560insGGGGGGGGGGGGGGGGGGGGG (HOXC11) MANE Select NP_055027.1:p.Ser187delinsTrpGlyGlyGlyGlyGlyGlyAla