Canonical Allele Identifier: CA2037241506
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973996G= , CM000674.2:g.53973996G= GRCh38
NC_000012.11:g.54367780G= , CM000674.1:g.54367780G= GRCh37
NC_000012.10:g.52654047G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.686+69G= (HOXC11) ENSP00000243082.4:n.686+69G=
ENST00000546378.1:c.682+73G= (HOXC11) MANE Select ENSP00000446680.1:n.682+73G=
NM_014212.3:c.682+73G= (HOXC11) NP_055027.1:n.682+73G=
NR_047517.1:n.59+902C= (HOTAIR)
NM_014212.4:c.682+73G= (HOXC11) MANE Select NP_055027.1:n.682+73G=