Canonical Allele Identifier: CA6156266
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs745779714

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648110C>T , CM000673.2:g.69648110C>T GRCh38
NC_000011.9:g.69462878C>T , CM000673.1:g.69462878C>T GRCh37
NC_000011.8:g.69172059C>T NCBI36
NG_007375.1:g.12006C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.691C>T MANE Select ENSP00000227507.2:p.Arg231Cys
ENST00000227507.2:c.691C>T ENSP00000227507.2:p.Arg231Cys
ENST00000536559.1:c.*111C>T ENSP00000438482.1:n.*111C>T
ENST00000542367.1:n.154C>T
ENST00000545484.1:n.397C>T
NM_053056.2:c.691C>T NP_444284.1:p.Arg231Cys
XM_006718653.2:c.715C>T XP_006718716.1:p.Arg239Cys
NM_053056.3:c.691C>T MANE Select NP_444284.1:p.Arg231Cys