Canonical Allele Identifier: CA2013094728

Gene: CCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4296139G= , CM000674.2:g.4296139G=	GRCh38
NC_000012.11:g.4405305G= , CM000674.1:g.4405305G=	GRCh37
NC_000012.10:g.4275566G=	NCBI36
NG_034254.1:g.27404G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.721-3721G= MANE Select	ENSP00000261254.3:n.721-3721G=
ENST00000536537.2:n.851-1618G=
ENST00000648100.1:c.720+7149G=	ENSP00000497536.1:n.720+7149G=
ENST00000674624.1:c.720+7149G=	ENSP00000501898.1:n.720+7149G=
ENST00000675468.1:n.645-3721G=
ENST00000675880.1:c.763-3721G=	ENSP00000502508.1:n.763-3721G=
ENST00000676279.1:c.721-3721G=	ENSP00000502597.1:n.721-3721G=
ENST00000676411.1:c.721-3721G=	ENSP00000502654.1:n.721-3721G=
ENST00000261254.7:c.721-3721G=	ENSP00000261254.3:n.721-3721G=
ENST00000536537.1:c.318-1618G=
NM_001759.3:c.721-3721G=	NP_001750.1:n.721-3721G=
NM_001759.4:c.721-3721G= MANE Select	NP_001750.1:n.721-3721G=