Canonical Allele Identifier: CA381658080
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109305
MyVariant Identifiers: chr11:g.69462840G>A (hg19) chr11:g.69648072G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648072G>A , CM000673.2:g.69648072G>A GRCh38
NC_000011.9:g.69462840G>A , CM000673.1:g.69462840G>A GRCh37
NC_000011.8:g.69172021G>A NCBI36
NG_007375.1:g.11968G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.653G>A MANE Select ENSP00000227507.2:p.Arg218Lys
ENST00000227507.2:c.653G>A ENSP00000227507.2:p.Arg218Lys
ENST00000536559.1:c.*73G>A ENSP00000438482.1:n.*73G>A
ENST00000542367.1:n.116G>A
ENST00000545484.1:n.359G>A
NM_053056.2:c.653G>A NP_444284.1:p.Arg218Lys
XM_006718653.2:c.677G>A XP_006718716.1:p.Arg226Lys
NM_053056.3:c.653G>A MANE Select NP_444284.1:p.Arg218Lys
Search 100 bp 5'
Search 100 bp 3'