Canonical Allele Identifier: CA170551

Gene: CCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4299978C>A , CM000674.2:g.4299978C>A	GRCh38
NC_000012.11:g.4409144C>A , CM000674.1:g.4409144C>A	GRCh37
NC_000012.10:g.4279405C>A	NCBI36
NG_034254.1:g.31243C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.839C>A MANE Select	ENSP00000261254.3:p.Thr280Asn
ENST00000648100.1:c.720+10988C>A	ENSP00000497536.1:n.720+10988C>A
ENST00000674624.1:c.720+10988C>A	ENSP00000501898.1:n.720+10988C>A
ENST00000675468.1:n.763C>A
ENST00000675880.1:c.881C>A	ENSP00000502508.1:p.Thr294Asn
ENST00000676279.1:c.839C>A	ENSP00000502597.1:p.Thr280Asn
ENST00000676411.1:c.839C>A	ENSP00000502654.1:p.Thr280Asn
ENST00000261254.7:c.839C>A	ENSP00000261254.3:p.Thr280Asn
NM_001759.3:c.839C>A	NP_001750.1:p.Thr280Asn
NM_001759.4:c.839C>A MANE Select	NP_001750.1:p.Thr280Asn