Canonical Allele Identifier: CA381657948
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120108657

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648008T>A , CM000673.2:g.69648008T>A GRCh38
NC_000011.9:g.69462776T>A , CM000673.1:g.69462776T>A GRCh37
NC_000011.8:g.69171957T>A NCBI36
NG_007375.1:g.11904T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.589T>A MANE Select ENSP00000227507.2:p.Ser197Thr
ENST00000227507.2:c.589T>A ENSP00000227507.2:p.Ser197Thr
ENST00000536559.1:c.*9T>A ENSP00000438482.1:n.*9T>A
ENST00000542367.1:n.52T>A
ENST00000545484.1:n.295T>A
NM_053056.2:c.589T>A NP_444284.1:p.Ser197Thr
XM_006718653.2:c.613T>A XP_006718716.1:p.Ser205Thr
NM_053056.3:c.589T>A MANE Select NP_444284.1:p.Ser197Thr