Canonical Allele Identifier: CA2013084080
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273493_4273494delinsGT , CM000674.2:g.4273493_4273494delinsGT GRCh38
NC_000012.11:g.4382659_4382660delinsGT , CM000674.1:g.4382659_4382660delinsGT GRCh37
NC_000012.10:g.4252920_4252921delinsGT NCBI36
NG_034254.1:g.4758_4759delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+240_-41+241delinsGT (CCND2) ENSP00000502597.1:n.-41+240_-41+241delinsGT
ENST00000676411.1:c.-40-508_-40-507delinsGT (CCND2) ENSP00000502654.1:n.-40-508_-40-507delinsGT
NR_125790.1:n.126+2565_126+2566delinsAC (CCND2-AS1)
NR_149145.1:n.182+1802_182+1803delinsAC (CCND2-AS1)
NR_149146.1:n.182+1802_182+1803delinsAC (CCND2-AS1)
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