Canonical Allele Identifier: CA381657912
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1855806261
MyVariant Identifiers: chr11:g.69462762A>C (hg19) chr11:g.69647994A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69647994A>C , CM000673.2:g.69647994A>C GRCh38
NC_000011.9:g.69462762A>C , CM000673.1:g.69462762A>C GRCh37
NC_000011.8:g.69171943A>C NCBI36
NG_007375.1:g.11890A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.575A>C MANE Select ENSP00000227507.2:p.Asp192Ala
ENST00000227507.2:c.575A>C ENSP00000227507.2:p.Asp192Ala
ENST00000536559.1:c.199A>C ENSP00000438482.1:p.Met67Leu
ENST00000542367.1:n.38A>C
ENST00000545484.1:n.281A>C
NM_053056.2:c.575A>C NP_444284.1:p.Asp192Ala
XM_006718653.2:c.599A>C XP_006718716.1:p.Asp200Ala
NM_053056.3:c.575A>C MANE Select NP_444284.1:p.Asp192Ala
Search 100 bp 5'
Search 100 bp 3'