Canonical Allele Identifier: CA2037241152
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973759G= , CM000674.2:g.53973759G= GRCh38
NC_000012.11:g.54367543G= , CM000674.1:g.54367543G= GRCh37
NC_000012.10:g.52653810G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.518G= (HOXC11) ENSP00000243082.4:p.Gly173=
ENST00000546378.1:c.518G= (HOXC11) MANE Select ENSP00000446680.1:p.Gly173=
NM_014212.3:c.518G= (HOXC11) NP_055027.1:p.Gly173=
NR_047517.1:n.59+1139C= (HOTAIR)
NM_014212.4:c.518G= (HOXC11) MANE Select NP_055027.1:p.Gly173=