Canonical Allele Identifier: CA2013084358
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1863820621

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273894_4273898del , CM000674.2:g.4273894_4273898del GRCh38
NC_000012.11:g.4383060_4383064del , CM000674.1:g.4383060_4383064del GRCh37
NC_000012.10:g.4253321_4253325del NCBI36
NG_034254.1:g.5159_5163del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261254.8:c.-147_-143del (CCND2) MANE Select ENSP00000261254.3:n.-147_-143del
ENST00000536537.2:n.133_137del (CCND2)
ENST00000648100.1:c.-147_-143del ENSP00000497536.1:n.-147_-143del
ENST00000674624.1:c.-147_-143del ENSP00000501898.1:n.-147_-143del
ENST00000675880.1:c.-147_-143del (CCND2) ENSP00000502508.1:n.-147_-143del
ENST00000676279.1:c.-40-107_-40-103del (CCND2) ENSP00000502597.1:n.-40-107_-40-103del
ENST00000676411.1:c.-40-107_-40-103del (CCND2) ENSP00000502654.1:n.-40-107_-40-103del
ENST00000261254.7:c.-147_-143del (CCND2) ENSP00000261254.3:n.-147_-143del
NM_001759.3:c.-147_-143del (CCND2) NP_001750.1:n.-147_-143del
NR_125790.1:n.126+2163_126+2167del (CCND2-AS1)
XM_005253813.3:c.-147_-143del (CCND2) XP_005253870.1:n.-147_-143del
NR_149145.1:n.182+1400_182+1404del (CCND2-AS1)
NR_149146.1:n.182+1400_182+1404del (CCND2-AS1)
NM_001759.4:c.-147_-143del (CCND2) MANE Select NP_001750.1:n.-147_-143del