Canonical Allele Identifier: CA2013084349
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273882_4273885delinsCCTT , CM000674.2:g.4273882_4273885delinsCCTT GRCh38
NC_000012.11:g.4383048_4383051delinsCCTT , CM000674.1:g.4383048_4383051delinsCCTT GRCh37
NC_000012.10:g.4253309_4253312delinsCCTT NCBI36
NG_034254.1:g.5147_5150delinsCCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000261254.8:c.-159_-156delinsCCTT (CCND2) MANE Select ENSP00000261254.3:n.-159_-156delinsCCTT
ENST00000536537.2:n.121_124delinsCCTT (CCND2)
ENST00000648100.1:c.-159_-156delinsCCTT ENSP00000497536.1:n.-159_-156delinsCCTT
ENST00000674624.1:c.-159_-156delinsCCTT ENSP00000501898.1:n.-159_-156delinsCCTT
ENST00000675880.1:c.-159_-156delinsCCTT (CCND2) ENSP00000502508.1:n.-159_-156delinsCCTT
ENST00000676279.1:c.-40-119_-40-116delinsCCTT (CCND2) ENSP00000502597.1:n.-40-119_-40-116delins...
ENST00000676411.1:c.-40-119_-40-116delinsCCTT (CCND2) ENSP00000502654.1:n.-40-119_-40-116delins...
ENST00000261254.7:c.-159_-156delinsCCTT (CCND2) ENSP00000261254.3:n.-159_-156delinsCCTT
NM_001759.3:c.-159_-156delinsCCTT (CCND2) NP_001750.1:n.-159_-156delinsCCTT
NR_125790.1:n.126+2174_126+2177delinsAAGG (CCND2-AS1)
XM_005253813.3:c.-159_-156delinsCCTT (CCND2) XP_005253870.1:n.-159_-156delinsCCTT
NR_149145.1:n.182+1411_182+1414delinsAAGG (CCND2-AS1)
NR_149146.1:n.182+1411_182+1414delinsAAGG (CCND2-AS1)
NM_001759.4:c.-159_-156delinsCCTT (CCND2) MANE Select NP_001750.1:n.-159_-156delinsCCTT