Canonical Allele Identifier: CA2792567571
Gene: CCND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648103_69648104insAACCAAACACACCCAA , CM000673.2:g.69648103_69648104insAACCAAACACACCCAA GRCh38
NC_000011.9:g.69462871_69462872insAACCAAACACACCCAA , CM000673.1:g.69462871_69462872insAACCAAACACACCCAA GRCh37
NC_000011.8:g.69172052_69172053insAACCAAACACACCCAA NCBI36
NG_007375.1:g.11999_12000insAACCAAACACACCCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.684_685insAACCAAACACACCCAA MANE Select ENSP00000227507.2:p.Leu229AsnfsTer17
ENST00000227507.2:c.684_685insAACCAAACACACCCAA ENSP00000227507.2:p.Leu229AsnfsTer17
ENST00000536559.1:c.*104_*105insAACCAAACACACCCAA ENSP00000438482.1:n.*104_*105insAACCAAACACACCCAA
ENST00000542367.1:n.147_148insAACCAAACACACCCAA
ENST00000545484.1:n.390_391insAACCAAACACACCCAA
NM_053056.2:c.684_685insAACCAAACACACCCAA NP_444284.1:p.Leu229AsnfsTer17
XM_006718653.2:c.708_709insAACCAAACACACCCAA XP_006718716.1:p.Leu237AsnfsTer17
NM_053056.3:c.684_685insAACCAAACACACCCAA MANE Select NP_444284.1:p.Leu229AsnfsTer17