Canonical Allele Identifier: CA2497327858
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1855834480

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69649978dup , CM000673.2:g.69649978dup GRCh38
NC_000011.9:g.69464746dup , CM000673.1:g.69464746dup GRCh37
NC_000011.8:g.69173927dup NCBI36
NG_007375.1:g.13874dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.724-1140dup MANE Select ENSP00000227507.2:n.724-1140dup
ENST00000227507.2:c.724-1140dup ENSP00000227507.2:n.724-1140dup
ENST00000542367.1:n.187-1140dup
NM_053056.2:c.724-1140dup NP_444284.1:n.724-1140dup
XM_006718653.2:c.748-1140dup XP_006718716.1:n.748-1140dup
NM_053056.3:c.724-1140dup MANE Select NP_444284.1:n.724-1140dup