Canonical Allele Identifier: CA381658165
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109901

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648113T>A , CM000673.2:g.69648113T>A GRCh38
NC_000011.9:g.69462881T>A , CM000673.1:g.69462881T>A GRCh37
NC_000011.8:g.69172062T>A NCBI36
NG_007375.1:g.12009T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.694T>A MANE Select ENSP00000227507.2:p.Phe232Ile
ENST00000227507.2:c.694T>A ENSP00000227507.2:p.Phe232Ile
ENST00000536559.1:c.*114T>A ENSP00000438482.1:n.*114T>A
ENST00000542367.1:n.157T>A
ENST00000545484.1:n.400T>A
NM_053056.2:c.694T>A NP_444284.1:p.Phe232Ile
XM_006718653.2:c.718T>A XP_006718716.1:p.Phe240Ile
NM_053056.3:c.694T>A MANE Select NP_444284.1:p.Phe232Ile