Canonical Allele Identifier: CA385105221
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

COSMIC: COSM5658175
MyVariant Identifiers: chr12:g.54367536T>C (hg19) chr12:g.53973752T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973752T>C , CM000674.2:g.53973752T>C GRCh38
NC_000012.11:g.54367536T>C , CM000674.1:g.54367536T>C GRCh37
NC_000012.10:g.52653803T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.511T>C (HOXC11) ENSP00000243082.4:p.Cys171Arg
ENST00000546378.1:c.511T>C (HOXC11) MANE Select ENSP00000446680.1:p.Cys171Arg
NM_014212.3:c.511T>C (HOXC11) NP_055027.1:p.Cys171Arg
NR_047517.1:n.59+1146A>G (HOTAIR)
NM_014212.4:c.511T>C (HOXC11) MANE Select NP_055027.1:p.Cys171Arg
Search 100 bp 5'
Search 100 bp 3'