Canonical Allele Identifier: CA2792567572
Gene: CCND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648127del , CM000673.2:g.69648127del GRCh38
NC_000011.9:g.69462895del , CM000673.1:g.69462895del GRCh37
NC_000011.8:g.69172076del NCBI36
NG_007375.1:g.12023del

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.708del MANE Select ENSP00000227507.2:p.Ile237SerfsTer?
ENST00000227507.2:c.708del ENSP00000227507.2:p.Ile237SerfsTer?
ENST00000536559.1:c.*128del ENSP00000438482.1:n.*128del
ENST00000542367.1:n.171del
ENST00000545484.1:n.414del
NM_053056.2:c.708del NP_444284.1:p.Ile237SerfsTer?
XM_006718653.2:c.732del XP_006718716.1:p.Ile245SerfsTer?
NM_053056.3:c.708del MANE Select NP_444284.1:p.Ile237SerfsTer?