Canonical Allele Identifier: CA385105113
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.54367515G>T (hg19) chr12:g.53973731G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973731G>T , CM000674.2:g.53973731G>T GRCh38
NC_000012.11:g.54367515G>T , CM000674.1:g.54367515G>T GRCh37
NC_000012.10:g.52653782G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.490G>T (HOXC11) ENSP00000243082.4:p.Asp164Tyr
ENST00000546378.1:c.490G>T (HOXC11) MANE Select ENSP00000446680.1:p.Asp164Tyr
NM_014212.3:c.490G>T (HOXC11) NP_055027.1:p.Asp164Tyr
NR_047517.1:n.59+1167C>A (HOTAIR)
NM_014212.4:c.490G>T (HOXC11) MANE Select NP_055027.1:p.Asp164Tyr
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