Canonical Allele Identifier: CA2037241280
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973838_53973844delinsGGAGGCT , CM000674.2:g.53973838_53973844delinsGGAGGCT GRCh38
NC_000012.11:g.54367622_54367628delinsGGAGGCT , CM000674.1:g.54367622_54367628delinsGGAGGCT GRCh37
NC_000012.10:g.52653889_52653895delinsGGAGGCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.597_603delinsGGAGGCT (HOXC11) ENSP00000243082.4:p.Ala199=
ENST00000546378.1:c.597_603delinsGGAGGCT (HOXC11) MANE Select ENSP00000446680.1:p.Ala199=
NM_014212.3:c.597_603delinsGGAGGCT (HOXC11) NP_055027.1:p.Ala199=
NR_047517.1:n.59+1054_59+1060delinsAGCCTCC (HOTAIR)
NM_014212.4:c.597_603delinsGGAGGCT (HOXC11) MANE Select NP_055027.1:p.Ala199=