Canonical Allele Identifier: CA939231259
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1855835009
gnomAD v3: 11-69650035-TG-T
gnomAD v4: 11-69650035-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69650037del , CM000673.2:g.69650037del GRCh38
NC_000011.9:g.69464805del , CM000673.1:g.69464805del GRCh37
NC_000011.8:g.69173986del NCBI36
NG_007375.1:g.13933del

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.724-1081del MANE Select ENSP00000227507.2:n.724-1081del
ENST00000227507.2:c.724-1081del ENSP00000227507.2:n.724-1081del
ENST00000542367.1:n.187-1081del
NM_053056.2:c.724-1081del NP_444284.1:n.724-1081del
XM_006718653.2:c.748-1081del XP_006718716.1:n.748-1081del
NM_053056.3:c.724-1081del MANE Select NP_444284.1:n.724-1081del
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