Canonical Allele Identifier: CA2497327857
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1669718634
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69649924_69649927del , CM000673.2:g.69649924_69649927del GRCh38
NC_000011.9:g.69464692_69464695del , CM000673.1:g.69464692_69464695del GRCh37
NC_000011.8:g.69173873_69173876del NCBI36
NG_007375.1:g.13820_13823del

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.724-1194_724-1191del MANE Select ENSP00000227507.2:n.724-1194_724-1191del
ENST00000227507.2:c.724-1194_724-1191del ENSP00000227507.2:n.724-1194_724-1191del
ENST00000542367.1:n.187-1194_187-1191del
NM_053056.2:c.724-1194_724-1191del NP_444284.1:n.724-1194_724-1191del
XM_006718653.2:c.748-1194_748-1191del XP_006718716.1:n.748-1194_748-1191del
NM_053056.3:c.724-1194_724-1191del MANE Select NP_444284.1:n.724-1194_724-1191del
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