Canonical Allele Identifier: CA2614780028
Gene: CCND1 HGNC NCBI

Linked Data

gnomAD v4: 11-69648215-CGAGGCTGGTGCCAAGGCCCCCAAGGGTGACAAGGTT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648217_69648252del , CM000673.2:g.69648217_69648252del GRCh38
NC_000011.9:g.69462985_69463020del , CM000673.1:g.69462985_69463020del GRCh37
NC_000011.8:g.69172166_69172201del NCBI36
NG_007375.1:g.12113_12148del

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+75_723+110del MANE Select ENSP00000227507.2:n.723+75_723+110del
ENST00000227507.2:c.723+75_723+110del ENSP00000227507.2:n.723+75_723+110del
ENST00000542367.1:n.186+75_186+110del
NM_053056.2:c.723+75_723+110del NP_444284.1:n.723+75_723+110del
XM_006718653.2:c.747+75_747+110del XP_006718716.1:n.747+75_747+110del
NM_053056.3:c.723+75_723+110del MANE Select NP_444284.1:n.723+75_723+110del
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