Canonical Allele Identifier: CA2069377563
Gene: NCOR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124549318_124549319delinsTC , CM000674.2:g.124549318_124549319delinsTC GRCh38
NC_000012.11:g.125033864_125033865delinsTC , CM000674.1:g.125033864_125033865delinsTC GRCh37
NC_000012.10:g.123599817_123599818delinsTC NCBI36
NG_022928.2:g.23146_23147delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000405201.6:c.-164-13708_-164-13707delinsGA MANE Select ENSP00000384018.1:n.-164-13708_-164-13707...
ENST00000458234.5:c.-164-13708_-164-13707delinsGA ENSP00000402808.1:n.-164-13708_-164-13707...
ENST00000542565.1:n.283-13708_283-13707delinsGA
NM_001077261.3:c.-164-13708_-164-13707delinsGA NP_001070729.2:n.-164-13708_-164-13707del...
NM_001206654.1:c.-164-13708_-164-13707delinsGA NP_001193583.1:n.-164-13708_-164-13707del...
NM_006312.5:c.-164-13708_-164-13707delinsGA NP_006303.4:n.-164-13708_-164-13707delins...
NM_001077261.4:c.-164-13708_-164-13707delinsGA NP_001070729.2:n.-164-13708_-164-13707del...
NM_001206654.2:c.-164-13708_-164-13707delinsGA NP_001193583.1:n.-164-13708_-164-13707del...
NM_006312.6:c.-164-13708_-164-13707delinsGA MANE Select NP_006303.4:n.-164-13708_-164-13707delins...