Canonical Allele Identifier: CA6395340

Gene: CCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4299988C>T , CM000674.2:g.4299988C>T	GRCh38
NC_000012.11:g.4409154C>T , CM000674.1:g.4409154C>T	GRCh37
NC_000012.10:g.4279415C>T	NCBI36
NG_034254.1:g.31253C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.849C>T MANE Select	ENSP00000261254.3:p.Asp283=
ENST00000648100.1:c.720+10998C>T	ENSP00000497536.1:n.720+10998C>T
ENST00000674624.1:c.720+10998C>T	ENSP00000501898.1:n.720+10998C>T
ENST00000675468.1:n.773C>T
ENST00000675880.1:c.891C>T	ENSP00000502508.1:p.Asp297=
ENST00000676279.1:c.849C>T	ENSP00000502597.1:p.Asp283=
ENST00000676411.1:c.849C>T	ENSP00000502654.1:p.Asp283=
ENST00000261254.7:c.849C>T	ENSP00000261254.3:p.Asp283=
NM_001759.3:c.849C>T	NP_001750.1:p.Asp283=
NM_001759.4:c.849C>T MANE Select	NP_001750.1:p.Asp283=