Canonical Allele Identifier: CA381657917
Gene: CCND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69462763T>G (hg19) chr11:g.69647995T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69647995T>G , CM000673.2:g.69647995T>G GRCh38
NC_000011.9:g.69462763T>G , CM000673.1:g.69462763T>G GRCh37
NC_000011.8:g.69171944T>G NCBI36
NG_007375.1:g.11891T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.576T>G MANE Select ENSP00000227507.2:p.Asp192Glu
ENST00000227507.2:c.576T>G ENSP00000227507.2:p.Asp192Glu
ENST00000536559.1:c.200T>G ENSP00000438482.1:p.Met67Arg
ENST00000542367.1:n.39T>G
ENST00000545484.1:n.282T>G
NM_053056.2:c.576T>G NP_444284.1:p.Asp192Glu
XM_006718653.2:c.600T>G XP_006718716.1:p.Asp200Glu
NM_053056.3:c.576T>G MANE Select NP_444284.1:p.Asp192Glu
Search 100 bp 5'
Search 100 bp 3'