Canonical Allele Identifier: CA2617154152
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273837_4273838insA , CM000674.2:g.4273837_4273838insA GRCh38
NC_000012.11:g.4383003_4383004insA , CM000674.1:g.4383003_4383004insA GRCh37
NC_000012.10:g.4253264_4253265insA NCBI36
NG_034254.1:g.5102_5103insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261254.8:c.-204_-203insA (CCND2) MANE Select ENSP00000261254.3:n.-204_-203insA
ENST00000536537.2:n.76_77insA (CCND2)
ENST00000648100.1:c.-204_-203insA ENSP00000497536.1:n.-204_-203insA
ENST00000674624.1:c.-204_-203insA ENSP00000501898.1:n.-204_-203insA
ENST00000675880.1:c.-204_-203insA (CCND2) ENSP00000502508.1:n.-204_-203insA
ENST00000676279.1:c.-40-164_-40-163insA (CCND2) ENSP00000502597.1:n.-40-164_-40-163insA
ENST00000676411.1:c.-40-164_-40-163insA (CCND2) ENSP00000502654.1:n.-40-164_-40-163insA
ENST00000261254.7:c.-204_-203insA (CCND2) ENSP00000261254.3:n.-204_-203insA
NM_001759.3:c.-204_-203insA (CCND2) NP_001750.1:n.-204_-203insA
NR_125790.1:n.126+2221_126+2222insT (CCND2-AS1)
XM_005253813.3:c.-204_-203insA (CCND2) XP_005253870.1:n.-204_-203insA
NR_149145.1:n.182+1458_182+1459insT (CCND2-AS1)
NR_149146.1:n.182+1458_182+1459insT (CCND2-AS1)
NM_001759.4:c.-204_-203insA (CCND2) MANE Select NP_001750.1:n.-204_-203insA