Canonical Allele Identifier: CA2069377565
Gene: NCOR2 HGNC NCBI

Linked Data

dbSNP Id: rs2051638762

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124549322_124549330del , CM000674.2:g.124549322_124549330del GRCh38
NC_000012.11:g.125033868_125033876del , CM000674.1:g.125033868_125033876del GRCh37
NC_000012.10:g.123599821_123599829del NCBI36
NG_022928.2:g.23137_23145del

Transcript Alleles

HGVS Amino-acid change
ENST00000405201.6:c.-164-13717_-164-13709del MANE Select ENSP00000384018.1:n.-164-13717_-164-13709...
ENST00000458234.5:c.-164-13717_-164-13709del ENSP00000402808.1:n.-164-13717_-164-13709...
ENST00000542565.1:n.283-13717_283-13709del
NM_001077261.3:c.-164-13717_-164-13709del NP_001070729.2:n.-164-13717_-164-13709del...
NM_001206654.1:c.-164-13717_-164-13709del NP_001193583.1:n.-164-13717_-164-13709del...
NM_006312.5:c.-164-13717_-164-13709del NP_006303.4:n.-164-13717_-164-13709del
NM_001077261.4:c.-164-13717_-164-13709del NP_001070729.2:n.-164-13717_-164-13709del...
NM_001206654.2:c.-164-13717_-164-13709del NP_001193583.1:n.-164-13717_-164-13709del...
NM_006312.6:c.-164-13717_-164-13709del MANE Select NP_006303.4:n.-164-13717_-164-13709del