Canonical Allele Identifier: CA475219514
Gene: CCND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69462799A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648031A>C , CM000673.2:g.69648031A>C GRCh38
NC_000011.9:g.69462799A>C , CM000673.1:g.69462799A>C GRCh37
NC_000011.8:g.69171980A>C NCBI36
NG_007375.1:g.11927A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.612A>C MANE Select ENSP00000227507.2:p.Ala204=
ENST00000227507.2:c.612A>C ENSP00000227507.2:p.Ala204=
ENST00000536559.1:c.*32A>C ENSP00000438482.1:n.*32A>C
ENST00000542367.1:n.75A>C
ENST00000545484.1:n.318A>C
NM_053056.2:c.612A>C NP_444284.1:p.Ala204=
XM_006718653.2:c.636A>C XP_006718716.1:p.Ala212=
NM_053056.3:c.612A>C MANE Select NP_444284.1:p.Ala204=
Search 100 bp 5'
Search 100 bp 3'