Canonical Allele Identifier: CA2013096639

Gene: CCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4299990T= , CM000674.2:g.4299990T=	GRCh38
NC_000012.11:g.4409156T= , CM000674.1:g.4409156T=	GRCh37
NC_000012.10:g.4279417T=	NCBI36
NG_034254.1:g.31255T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001759.4:c.851T= MANE Select	NP_001750.1:p.Val284=
ENST00000261254.8:c.851T= MANE Select	ENSP00000261254.3:p.Val284=
NM_001759.3:c.851T=	NP_001750.1:p.Val284=
ENST00000261254.7:c.851T=	ENSP00000261254.3:p.Val284=
ENST00000648100.1:c.720+11000T=	ENSP00000497536.1:n.720+11000T=
ENST00000674624.1:c.720+11000T=	ENSP00000501898.1:n.720+11000T=
ENST00000675468.1:n.775T=
ENST00000675880.1:c.893T=	ENSP00000502508.1:p.Val298=
ENST00000676279.1:c.851T=	ENSP00000502597.1:p.Val284=
ENST00000676411.1:c.851T=	ENSP00000502654.1:p.Val284=