Canonical Allele Identifier: CA2619096664
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973826_53973843del , CM000674.2:g.53973826_53973843del GRCh38
NC_000012.11:g.54367610_54367627del , CM000674.1:g.54367610_54367627del GRCh37
NC_000012.10:g.52653877_52653894del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.585_602del (HOXC11) ENSP00000243082.4:p.Gly196_Ala201del
ENST00000546378.1:c.585_602del (HOXC11) MANE Select ENSP00000446680.1:p.Gly196_Ala201del
NM_014212.3:c.585_602del (HOXC11) NP_055027.1:p.Gly196_Ala201del
NR_047517.1:n.59+1060_59+1077del (HOTAIR)
NM_014212.4:c.585_602del (HOXC11) MANE Select NP_055027.1:p.Gly196_Ala201del