Canonical Allele Identifier: CA2614780011
Gene: CCND1 HGNC NCBI

Linked Data

gnomAD v4: 11-69648175-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648179del , CM000673.2:g.69648179del GRCh38
NC_000011.9:g.69462947del , CM000673.1:g.69462947del GRCh37
NC_000011.8:g.69172128del NCBI36
NG_007375.1:g.12075del

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+37del MANE Select ENSP00000227507.2:n.723+37del
ENST00000227507.2:c.723+37del ENSP00000227507.2:n.723+37del
ENST00000536559.1:c.*180del ENSP00000438482.1:n.*180del
ENST00000542367.1:n.186+37del
NM_053056.2:c.723+37del NP_444284.1:n.723+37del
XM_006718653.2:c.747+37del XP_006718716.1:n.747+37del
NM_053056.3:c.723+37del MANE Select NP_444284.1:n.723+37del
Search 100 bp 5'
Search 100 bp 3'