Canonical Allele Identifier: CA385105952
Gene: HOXC11 HGNC NCBI
HOTAIR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53973891T>C , CM000674.2:g.53973891T>C GRCh38
NC_000012.11:g.54367675T>C , CM000674.1:g.54367675T>C GRCh37
NC_000012.10:g.52653942T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000243082.4:c.650T>C (HOXC11) ENSP00000243082.4:p.Val217Ala
ENST00000546378.1:c.650T>C (HOXC11) MANE Select ENSP00000446680.1:p.Val217Ala
NM_014212.3:c.650T>C (HOXC11) NP_055027.1:p.Val217Ala
NR_047517.1:n.59+1007A>G (HOTAIR)
NM_014212.4:c.650T>C (HOXC11) MANE Select NP_055027.1:p.Val217Ala