Canonical Allele Identifier: CA385105331
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

dbSNP Id: rs1555180022

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973769_53973770insT , CM000674.2:g.53973769_53973770insT GRCh38
NC_000012.11:g.54367553_54367554insT , CM000674.1:g.54367553_54367554insT GRCh37
NC_000012.10:g.52653820_52653821insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.528_529insT (HOXC11) ENSP00000243082.4:p.Ala177CysfsTer18
ENST00000546378.1:c.528_529insT (HOXC11) MANE Select ENSP00000446680.1:p.Ala177CysfsTer18
NM_014212.3:c.528_529insT (HOXC11) NP_055027.1:p.Ala177CysfsTer18
NR_047517.1:n.59+1128_59+1129insA (HOTAIR)
NM_014212.4:c.528_529insT (HOXC11) MANE Select NP_055027.1:p.Ala177CysfsTer18