Canonical Allele Identifier: CA123434
Gene: CCND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13755
dbSNP Id: rs9344

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648142G>A , CM000673.2:g.69648142G>A GRCh38
NC_000011.9:g.69462910G>A , CM000673.1:g.69462910G>A GRCh37
NC_000011.8:g.69172091G>A NCBI36
NG_007375.1:g.12038G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.723G>A MANE Select ENSP00000227507.2:p.Pro241=
ENST00000227507.2:c.723G>A ENSP00000227507.2:p.Pro241=
ENST00000536559.1:c.*143G>A ENSP00000438482.1:n.*143G>A
ENST00000542367.1:n.186G>A
ENST00000545484.1:n.429G>A
NM_053056.2:c.723G>A NP_444284.1:p.Pro241=
XM_006718653.2:c.747G>A XP_006718716.1:p.Pro249=
NM_053056.3:c.723G>A MANE Select NP_444284.1:p.Pro241=