Canonical Allele Identifier: CA2614779996
Gene: CCND1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648096_69648097insATGATACGG , CM000673.2:g.69648096_69648097insATGATACGG GRCh38
NC_000011.9:g.69462864_69462865insATGATACGG , CM000673.1:g.69462864_69462865insATGATACGG GRCh37
NC_000011.8:g.69172045_69172046insATGATACGG NCBI36
NG_007375.1:g.11992_11993insATGATACGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.677_678insATGATACGG MANE Select ENSP00000227507.2:p.Tyr226Ter
ENST00000227507.2:c.677_678insATGATACGG ENSP00000227507.2:p.Tyr226Ter
ENST00000536559.1:c.*97_*98insATGATACGG ENSP00000438482.1:n.*97_*98insATGATACGG
ENST00000542367.1:n.140_141insATGATACGG
ENST00000545484.1:n.383_384insATGATACGG
NM_053056.2:c.677_678insATGATACGG NP_444284.1:p.Tyr226Ter
XM_006718653.2:c.701_702insATGATACGG XP_006718716.1:p.Tyr234Ter
NM_053056.3:c.677_678insATGATACGG MANE Select NP_444284.1:p.Tyr226Ter