Canonical Allele Identifier: CA6156253
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs756509430

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648050G>A , CM000673.2:g.69648050G>A GRCh38
NC_000011.9:g.69462818G>A , CM000673.1:g.69462818G>A GRCh37
NC_000011.8:g.69171999G>A NCBI36
NG_007375.1:g.11946G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.631G>A MANE Select ENSP00000227507.2:p.Ala211Thr
ENST00000227507.2:c.631G>A ENSP00000227507.2:p.Ala211Thr
ENST00000536559.1:c.*51G>A ENSP00000438482.1:n.*51G>A
ENST00000542367.1:n.94G>A
ENST00000545484.1:n.337G>A
NM_053056.2:c.631G>A NP_444284.1:p.Ala211Thr
XM_006718653.2:c.655G>A XP_006718716.1:p.Ala219Thr
NM_053056.3:c.631G>A MANE Select NP_444284.1:p.Ala211Thr