Canonical Allele Identifier: CA2037241100
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973700_53973703delinsTTTC , CM000674.2:g.53973700_53973703delinsTTTC GRCh38
NC_000012.11:g.54367484_54367487delinsTTTC , CM000674.1:g.54367484_54367487delinsTTTC GRCh37
NC_000012.10:g.52653751_52653754delinsTTTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.459_462delinsTTTC (HOXC11) ENSP00000243082.4:p.Arg153=
ENST00000546378.1:c.459_462delinsTTTC (HOXC11) MANE Select ENSP00000446680.1:p.Arg153=
NM_014212.3:c.459_462delinsTTTC (HOXC11) NP_055027.1:p.Arg153=
NR_047517.1:n.59+1195_59+1198delinsGAAA (HOTAIR)
NM_014212.4:c.459_462delinsTTTC (HOXC11) MANE Select NP_055027.1:p.Arg153=