Canonical Allele Identifier: CA689961572
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

dbSNP Id: rs1205002923

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973766_53973777dup , CM000674.2:g.53973766_53973777dup GRCh38
NC_000012.11:g.54367550_54367561dup , CM000674.1:g.54367550_54367561dup GRCh37
NC_000012.10:g.52653817_52653828dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.525_536dup (HOXC11) ENSP00000243082.4:p.Gly179_Glu180insGluAlaLysGly
ENST00000546378.1:c.525_536dup (HOXC11) MANE Select ENSP00000446680.1:p.Gly179_Glu180insGluAlaLysGly
NM_014212.3:c.525_536dup (HOXC11) NP_055027.1:p.Gly179_Glu180insGluAlaLysGly
NR_047517.1:n.59+1127_59+1138dup (HOTAIR)
NM_014212.4:c.525_536dup (HOXC11) MANE Select NP_055027.1:p.Gly179_Glu180insGluAlaLysGly