Canonical Allele Identifier: CA2037241289
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973844_53973847delinsTGAG , CM000674.2:g.53973844_53973847delinsTGAG GRCh38
NC_000012.11:g.54367628_54367631delinsTGAG , CM000674.1:g.54367628_54367631delinsTGAG GRCh37
NC_000012.10:g.52653895_52653898delinsTGAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.603_606delinsTGAG (HOXC11) ENSP00000243082.4:p.Ala201=
ENST00000546378.1:c.603_606delinsTGAG (HOXC11) MANE Select ENSP00000446680.1:p.Ala201=
NM_014212.3:c.603_606delinsTGAG (HOXC11) NP_055027.1:p.Ala201=
NR_047517.1:n.59+1051_59+1054delinsCTCA (HOTAIR)
NM_014212.4:c.603_606delinsTGAG (HOXC11) MANE Select NP_055027.1:p.Ala201=