Canonical Allele Identifier: CA6395248

Gene: CCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4278852C>T , CM000674.2:g.4278852C>T	GRCh38
NC_000012.11:g.4388018C>T , CM000674.1:g.4388018C>T	GRCh37
NC_000012.10:g.4258279C>T	NCBI36
NG_034254.1:g.10117C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.504C>T MANE Select	ENSP00000261254.3:p.Pro168=
ENST00000536537.2:n.783C>T
ENST00000648100.1:c.504C>T	ENSP00000497536.1:p.Pro168=
ENST00000674624.1:c.504C>T	ENSP00000501898.1:p.Pro168=
ENST00000675468.1:n.428C>T
ENST00000675880.1:c.504C>T	ENSP00000502508.1:p.Pro168=
ENST00000676279.1:c.504C>T	ENSP00000502597.1:p.Pro168=
ENST00000676411.1:c.504C>T	ENSP00000502654.1:p.Pro168=
ENST00000261254.7:c.504C>T	ENSP00000261254.3:p.Pro168=
ENST00000536537.1:c.250C>T
ENST00000536795.1:n.185C>T
ENST00000541542.1:n.53C>T
NM_001759.3:c.504C>T	NP_001750.1:p.Pro168=
XM_005253813.3:c.504C>T	XP_005253870.1:p.Pro168=
NM_001759.4:c.504C>T MANE Select	NP_001750.1:p.Pro168=