Canonical Allele Identifier: CA2037241259
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973821G= , CM000674.2:g.53973821G= GRCh38
NC_000012.11:g.54367605G= , CM000674.1:g.54367605G= GRCh37
NC_000012.10:g.52653872G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.580G= (HOXC11) ENSP00000243082.4:p.Glu194=
ENST00000546378.1:c.580G= (HOXC11) MANE Select ENSP00000446680.1:p.Glu194=
NM_014212.3:c.580G= (HOXC11) NP_055027.1:p.Glu194=
NR_047517.1:n.59+1077C= (HOTAIR)
NM_014212.4:c.580G= (HOXC11) MANE Select NP_055027.1:p.Glu194=