Canonical Allele Identifier: CA381658190
Gene: CCND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69462892A>C (hg19) chr11:g.69648124A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648124A>C , CM000673.2:g.69648124A>C GRCh38
NC_000011.9:g.69462892A>C , CM000673.1:g.69462892A>C GRCh37
NC_000011.8:g.69172073A>C NCBI36
NG_007375.1:g.12020A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.705A>C MANE Select ENSP00000227507.2:p.Arg235Ser
ENST00000227507.2:c.705A>C ENSP00000227507.2:p.Arg235Ser
ENST00000536559.1:c.*125A>C ENSP00000438482.1:n.*125A>C
ENST00000542367.1:n.168A>C
ENST00000545484.1:n.411A>C
NM_053056.2:c.705A>C NP_444284.1:p.Arg235Ser
XM_006718653.2:c.729A>C XP_006718716.1:p.Arg243Ser
NM_053056.3:c.705A>C MANE Select NP_444284.1:p.Arg235Ser
Search 100 bp 5'
Search 100 bp 3'