Canonical Allele Identifier: CA2037241196
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973780_53973808delinsAGCCCGAGGCACCCCCGGCCTCGGGACTG , CM000674.2:g.53973780_53973808delinsAGCCCGAGGCACCCCCGGCCTCGGGACTG GRCh38
NC_000012.11:g.54367564_54367592delinsAGCCCGAGGCACCCCCGGCCTCGGGACTG , CM000674.1:g.54367564_54367592delinsAGCCCGAGGCACCCCCGGCCTCGGGACTG GRCh37
NC_000012.10:g.52653831_52653859delinsAGCCCGAGGCACCCCCGGCCTCGGGACTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.539_567delinsAGCCCGAGGCACCCCCGGCCTCGGGACTG (HOXC11) ENSP00000243082.4:p.Glu180=
ENST00000546378.1:c.539_567delinsAGCCCGAGGCACCCCCGGCCTCGGGACTG (HOXC11) MANE Select ENSP00000446680.1:p.Glu180=
NM_014212.3:c.539_567delinsAGCCCGAGGCACCCCCGGCCTCGGGACTG (HOXC11) NP_055027.1:p.Glu180=
NR_047517.1:n.59+1090_59+1118delinsCAGTCCCGAGGCCGGGGGTGCCTCGGGCT (HOTAIR)
NM_014212.4:c.539_567delinsAGCCCGAGGCACCCCCGGCCTCGGGACTG (HOXC11) MANE Select NP_055027.1:p.Glu180=