Canonical Allele Identifier: CA2037241282
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

dbSNP Id: rs1939197153

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973843_53973848del , CM000674.2:g.53973843_53973848del GRCh38
NC_000012.11:g.54367627_54367632del , CM000674.1:g.54367627_54367632del GRCh37
NC_000012.10:g.52653894_52653899del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.602_607del (HOXC11) ENSP00000243082.4:p.Ala201_Glu202del
ENST00000546378.1:c.602_607del (HOXC11) MANE Select ENSP00000446680.1:p.Ala201_Glu202del
NM_014212.3:c.602_607del (HOXC11) NP_055027.1:p.Ala201_Glu202del
NR_047517.1:n.59+1054_59+1059del (HOTAIR)
NM_014212.4:c.602_607del (HOXC11) MANE Select NP_055027.1:p.Ala201_Glu202del