Canonical Allele Identifier: CA919091698
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

dbSNP Id: rs1592196150

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973799_53973819del , CM000674.2:g.53973799_53973819del GRCh38
NC_000012.11:g.54367583_54367603del , CM000674.1:g.54367583_54367603del GRCh37
NC_000012.10:g.52653850_52653870del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.558_578del (HOXC11) ENSP00000243082.4:p.Ser187_Ala193del
ENST00000546378.1:c.558_578del (HOXC11) MANE Select ENSP00000446680.1:p.Ser187_Ala193del
NM_014212.3:c.558_578del (HOXC11) NP_055027.1:p.Ser187_Ala193del
NR_047517.1:n.59+1082_59+1102del (HOTAIR)
NM_014212.4:c.558_578del (HOXC11) MANE Select NP_055027.1:p.Ser187_Ala193del