Canonical Allele Identifier: CA13386456

Gene: CCND1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69650025G>A , CM000673.2:g.69650025G>A	GRCh38
NC_000011.9:g.69464793G>A , CM000673.1:g.69464793G>A	GRCh37
NC_000011.8:g.69173974G>A	NCBI36
NG_007375.1:g.13921G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.724-1093G>A MANE Select	ENSP00000227507.2:n.724-1093G>A
ENST00000227507.2:c.724-1093G>A	ENSP00000227507.2:n.724-1093G>A
ENST00000542367.1:n.187-1093G>A
NM_053056.2:c.724-1093G>A	NP_444284.1:n.724-1093G>A
XM_006718653.2:c.748-1093G>A	XP_006718716.1:n.748-1093G>A
NM_053056.3:c.724-1093G>A MANE Select	NP_444284.1:n.724-1093G>A