Canonical Allele Identifier: CA2013084359

Gene: CCND2 CCND2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4273893T= , CM000674.2:g.4273893T=	GRCh38
NC_000012.11:g.4383059T= , CM000674.1:g.4383059T=	GRCh37
NC_000012.10:g.4253320T=	NCBI36
NG_034254.1:g.5158T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.-148T= (CCND2) MANE Select	ENSP00000261254.3:n.-148T=
ENST00000536537.2:n.132T= (CCND2)
ENST00000648100.1:c.-148T=	ENSP00000497536.1:n.-148T=
ENST00000674624.1:c.-148T=	ENSP00000501898.1:n.-148T=
ENST00000675880.1:c.-148T= (CCND2)	ENSP00000502508.1:n.-148T=
ENST00000676279.1:c.-40-108T= (CCND2)	ENSP00000502597.1:n.-40-108T=
ENST00000676411.1:c.-40-108T= (CCND2)	ENSP00000502654.1:n.-40-108T=
ENST00000261254.7:c.-148T= (CCND2)	ENSP00000261254.3:n.-148T=
NM_001759.3:c.-148T= (CCND2)	NP_001750.1:n.-148T=
NR_125790.1:n.126+2166A= (CCND2-AS1)
XM_005253813.3:c.-148T= (CCND2)	XP_005253870.1:n.-148T=
NR_149145.1:n.182+1403A= (CCND2-AS1)
NR_149146.1:n.182+1403A= (CCND2-AS1)
NM_001759.4:c.-148T= (CCND2) MANE Select	NP_001750.1:n.-148T=