Canonical Allele Identifier: CA381658157
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109800

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648107A>T , CM000673.2:g.69648107A>T GRCh38
NC_000011.9:g.69462875A>T , CM000673.1:g.69462875A>T GRCh37
NC_000011.8:g.69172056A>T NCBI36
NG_007375.1:g.12003A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.688A>T MANE Select ENSP00000227507.2:p.Thr230Ser
ENST00000227507.2:c.688A>T ENSP00000227507.2:p.Thr230Ser
ENST00000536559.1:c.*108A>T ENSP00000438482.1:n.*108A>T
ENST00000542367.1:n.151A>T
ENST00000545484.1:n.394A>T
NM_053056.2:c.688A>T NP_444284.1:p.Thr230Ser
XM_006718653.2:c.712A>T XP_006718716.1:p.Thr238Ser
NM_053056.3:c.688A>T MANE Select NP_444284.1:p.Thr230Ser