Canonical Allele Identifier: CA383661588

Gene: CCND2 CCND2-AS1

Linked Data

• MyVariant Identifiers: chr12:g.4383283T>G (hg19) ; chr12:g.4274117T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4274117T>G , CM000674.2:g.4274117T>G	GRCh38
NC_000012.11:g.4383283T>G , CM000674.1:g.4383283T>G	GRCh37
NC_000012.10:g.4253544T>G	NCBI36
NG_034254.1:g.5382T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.77T>G (CCND2) MANE Select	ENSP00000261254.3:p.Val26Gly
ENST00000536537.2:n.356T>G (CCND2)
ENST00000648100.1:c.77T>G	ENSP00000497536.1:p.Val26Gly
ENST00000674624.1:c.77T>G	ENSP00000501898.1:p.Val26Gly
ENST00000675880.1:c.77T>G (CCND2)	ENSP00000502508.1:p.Val26Gly
ENST00000676279.1:c.77T>G (CCND2)	ENSP00000502597.1:p.Val26Gly
ENST00000676411.1:c.77T>G (CCND2)	ENSP00000502654.1:p.Val26Gly
ENST00000261254.7:c.77T>G (CCND2)	ENSP00000261254.3:p.Val26Gly
NM_001759.3:c.77T>G (CCND2)	NP_001750.1:p.Val26Gly
NR_125790.1:n.126+1942A>C (CCND2-AS1)
XM_005253813.3:c.77T>G (CCND2)	XP_005253870.1:p.Val26Gly
NR_149145.1:n.182+1179A>C (CCND2-AS1)
NR_149146.1:n.182+1179A>C (CCND2-AS1)
NM_001759.4:c.77T>G (CCND2) MANE Select	NP_001750.1:p.Val26Gly