Canonical Allele Identifier: CA381658126
Gene: CCND1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648093C>A , CM000673.2:g.69648093C>A GRCh38
NC_000011.9:g.69462861C>A , CM000673.1:g.69462861C>A GRCh37
NC_000011.8:g.69172042C>A NCBI36
NG_007375.1:g.11989C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.674C>A MANE Select ENSP00000227507.2:p.Ser225Tyr
ENST00000227507.2:c.674C>A ENSP00000227507.2:p.Ser225Tyr
ENST00000536559.1:c.*94C>A ENSP00000438482.1:n.*94C>A
ENST00000542367.1:n.137C>A
ENST00000545484.1:n.380C>A
NM_053056.2:c.674C>A NP_444284.1:p.Ser225Tyr
XM_006718653.2:c.698C>A XP_006718716.1:p.Ser233Tyr
NM_053056.3:c.674C>A MANE Select NP_444284.1:p.Ser225Tyr