Canonical Allele Identifier: CA944199142

Gene: CCND2 CCND2-AS1

Linked Data

• gnomAD v3: 12-4273555-T-TGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
• gnomAD v4: 12-4273555-T-TGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4273561_4273562insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000674.2:g.4273561_4273562insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000012.11:g.4382727_4382728insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000674.1:g.4382727_4382728insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000012.10:g.4252988_4252989insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	NCBI36
NG_034254.1:g.4826_4827insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000676279.1:c.-41+308_-41+309insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG (CCND2)	ENSP00000502597.1:n.-41+308_-41+309insGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000676411.1:c.-40-440_-40-439insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG (CCND2)	ENSP00000502654.1:n.-40-440_-40-439insGGGGGGGGGGGGGGGGGGGGGGG...
NR_125790.1:n.126+2503_126+2504insCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC (CCND2-AS1)
NR_149145.1:n.182+1740_182+1741insCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC (CCND2-AS1)
NR_149146.1:n.182+1740_182+1741insCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC (CCND2-AS1)