Canonical Allele Identifier: CA231747582

Gene: CCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4300180C>T , CM000674.2:g.4300180C>T	GRCh38
NC_000012.11:g.4409346C>T , CM000674.1:g.4409346C>T	GRCh37
NC_000012.10:g.4279607C>T	NCBI36
NG_034254.1:g.31445C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001759.4:c.*171C>T MANE Select	NP_001750.1:n.*171C>T
ENST00000261254.8:c.*171C>T MANE Select	ENSP00000261254.3:n.*171C>T
NM_001759.3:c.*171C>T	NP_001750.1:n.*171C>T
ENST00000261254.7:c.*171C>T	ENSP00000261254.3:n.*171C>T
ENST00000648100.1:c.720+11190C>T	ENSP00000497536.1:n.720+11190C>T
ENST00000674624.1:c.720+11190C>T	ENSP00000501898.1:n.720+11190C>T
ENST00000675468.1:n.965C>T
ENST00000675880.1:c.*171C>T	ENSP00000502508.1:n.*171C>T
ENST00000676279.1:c.*171C>T	ENSP00000502597.1:n.*171C>T
ENST00000676411.1:c.*171C>T	ENSP00000502654.1:n.*171C>T