Canonical Allele Identifier: CA2619096633
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973812_53973815del , CM000674.2:g.53973812_53973815del GRCh38
NC_000012.11:g.54367596_54367599del , CM000674.1:g.54367596_54367599del GRCh37
NC_000012.10:g.52653863_52653866del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.571_574del (HOXC11) ENSP00000243082.4:p.Ser191GlyfsTer?
ENST00000546378.1:c.571_574del (HOXC11) MANE Select ENSP00000446680.1:p.Ser191GlyfsTer?
NM_014212.3:c.571_574del (HOXC11) NP_055027.1:p.Ser191GlyfsTer?
NR_047517.1:n.59+1083_59+1086del (HOTAIR)
NM_014212.4:c.571_574del (HOXC11) MANE Select NP_055027.1:p.Ser191GlyfsTer?