Canonical Allele Identifier: CA2013084294
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273786_4273790delinsAGAGC , CM000674.2:g.4273786_4273790delinsAGAGC GRCh38
NC_000012.11:g.4382952_4382956delinsAGAGC , CM000674.1:g.4382952_4382956delinsAGAGC GRCh37
NC_000012.10:g.4253213_4253217delinsAGAGC NCBI36
NG_034254.1:g.5051_5055delinsAGAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261254.8:c.-255_-251delinsAGAGC (CCND2) MANE Select ENSP00000261254.3:n.-255_-251delinsAGAGC
ENST00000536537.2:n.25_29delinsAGAGC (CCND2)
ENST00000648100.1:c.-255_-251delinsAGAGC ENSP00000497536.1:n.-255_-251delinsAGAGC
ENST00000674624.1:c.-255_-251delinsAGAGC ENSP00000501898.1:n.-255_-251delinsAGAGC
ENST00000675880.1:c.-255_-251delinsAGAGC (CCND2) ENSP00000502508.1:n.-255_-251delinsAGAGC
ENST00000676279.1:c.-40-215_-40-211delinsAGAGC (CCND2) ENSP00000502597.1:n.-40-215_-40-211delinsAGAGC
ENST00000676411.1:c.-40-215_-40-211delinsAGAGC (CCND2) ENSP00000502654.1:n.-40-215_-40-211delinsAGAGC
ENST00000261254.7:c.-255_-251delinsAGAGC (CCND2) ENSP00000261254.3:n.-255_-251delinsAGAGC
NM_001759.3:c.-255_-251delinsAGAGC (CCND2) NP_001750.1:n.-255_-251delinsAGAGC
NR_125790.1:n.126+2269_126+2273delinsGCTCT (CCND2-AS1)
XM_005253813.3:c.-255_-251delinsAGAGC (CCND2) XP_005253870.1:n.-255_-251delinsAGAGC
NR_149145.1:n.182+1506_182+1510delinsGCTCT (CCND2-AS1)
NR_149146.1:n.182+1506_182+1510delinsGCTCT (CCND2-AS1)
NM_001759.4:c.-255_-251delinsAGAGC (CCND2) MANE Select NP_001750.1:n.-255_-251delinsAGAGC