Canonical Allele Identifier: CA2794362683
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273890_4273893del , CM000674.2:g.4273890_4273893del GRCh38
NC_000012.11:g.4383056_4383059del , CM000674.1:g.4383056_4383059del GRCh37
NC_000012.10:g.4253317_4253320del NCBI36
NG_034254.1:g.5155_5158del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261254.8:c.-151_-148del (CCND2) MANE Select ENSP00000261254.3:n.-151_-148del
ENST00000536537.2:n.129_132del (CCND2)
ENST00000648100.1:c.-151_-148del ENSP00000497536.1:n.-151_-148del
ENST00000674624.1:c.-151_-148del ENSP00000501898.1:n.-151_-148del
ENST00000675880.1:c.-151_-148del (CCND2) ENSP00000502508.1:n.-151_-148del
ENST00000676279.1:c.-40-111_-40-108del (CCND2) ENSP00000502597.1:n.-40-111_-40-108del
ENST00000676411.1:c.-40-111_-40-108del (CCND2) ENSP00000502654.1:n.-40-111_-40-108del
ENST00000261254.7:c.-151_-148del (CCND2) ENSP00000261254.3:n.-151_-148del
NM_001759.3:c.-151_-148del (CCND2) NP_001750.1:n.-151_-148del
NR_125790.1:n.126+2171_126+2174del (CCND2-AS1)
XM_005253813.3:c.-151_-148del (CCND2) XP_005253870.1:n.-151_-148del
NR_149145.1:n.182+1408_182+1411del (CCND2-AS1)
NR_149146.1:n.182+1408_182+1411del (CCND2-AS1)
NM_001759.4:c.-151_-148del (CCND2) MANE Select NP_001750.1:n.-151_-148del
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