Canonical Allele Identifier: CA2792567657

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69649930A>G , CM000673.2:g.69649930A>G	GRCh38
NC_000011.9:g.69464698A>G , CM000673.1:g.69464698A>G	GRCh37
NC_000011.8:g.69173879A>G	NCBI36
NG_007375.1:g.13826A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000227507.3:c.724-1188A>G MANE Select	ENSP00000227507.2:n.724-1188A>G
ENST00000227507.2:c.724-1188A>G	ENSP00000227507.2:n.724-1188A>G
ENST00000542367.1:n.187-1188A>G
NM_053056.2:c.724-1188A>G	NP_444284.1:n.724-1188A>G
XM_006718653.2:c.748-1188A>G	XP_006718716.1:n.748-1188A>G
NM_053056.3:c.724-1188A>G MANE Select	NP_444284.1:n.724-1188A>G