Canonical Allele Identifier: CA2037241389
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973918C= , CM000674.2:g.53973918C= GRCh38
NC_000012.11:g.54367702C= , CM000674.1:g.54367702C= GRCh37
NC_000012.10:g.52653969C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.677C= (HOXC11) ENSP00000243082.4:p.Ala226=
ENST00000546378.1:c.677C= (HOXC11) MANE Select ENSP00000446680.1:p.Ala226=
NM_014212.3:c.677C= (HOXC11) NP_055027.1:p.Ala226=
NR_047517.1:n.59+980G= (HOTAIR)
NM_014212.4:c.677C= (HOXC11) MANE Select NP_055027.1:p.Ala226=
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