Canonical Allele Identifier: CA605245031
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

dbSNP Id: rs1442156378

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973936G>C , CM000674.2:g.53973936G>C GRCh38
NC_000012.11:g.54367720G>C , CM000674.1:g.54367720G>C GRCh37
NC_000012.10:g.52653987G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.686+9G>C (HOXC11) ENSP00000243082.4:n.686+9G>C
ENST00000546378.1:c.682+13G>C (HOXC11) MANE Select ENSP00000446680.1:n.682+13G>C
NM_014212.3:c.682+13G>C (HOXC11) NP_055027.1:n.682+13G>C
NR_047517.1:n.59+962C>G (HOTAIR)
NM_014212.4:c.682+13G>C (HOXC11) MANE Select NP_055027.1:n.682+13G>C