Canonical Allele Identifier: CA2037241276
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

dbSNP Id: rs1740947578

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973838_53973843dup , CM000674.2:g.53973838_53973843dup GRCh38
NC_000012.11:g.54367622_54367627dup , CM000674.1:g.54367622_54367627dup GRCh37
NC_000012.10:g.52653889_52653894dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.597_602dup (HOXC11) ENSP00000243082.4:p.Ala201_Glu202insGluAla
ENST00000546378.1:c.597_602dup (HOXC11) MANE Select ENSP00000446680.1:p.Ala201_Glu202insGluAla
NM_014212.3:c.597_602dup (HOXC11) NP_055027.1:p.Ala201_Glu202insGluAla
NR_047517.1:n.59+1060_59+1065dup (HOTAIR)
NM_014212.4:c.597_602dup (HOXC11) MANE Select NP_055027.1:p.Ala201_Glu202insGluAla