Canonical Allele Identifier: CA381658020
Gene: CCND1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648042T>C , CM000673.2:g.69648042T>C GRCh38
NC_000011.9:g.69462810T>C , CM000673.1:g.69462810T>C GRCh37
NC_000011.8:g.69171991T>C NCBI36
NG_007375.1:g.11938T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.623T>C MANE Select ENSP00000227507.2:p.Val208Ala
ENST00000227507.2:c.623T>C ENSP00000227507.2:p.Val208Ala
ENST00000536559.1:c.*43T>C ENSP00000438482.1:n.*43T>C
ENST00000542367.1:n.86T>C
ENST00000545484.1:n.329T>C
NM_053056.2:c.623T>C NP_444284.1:p.Val208Ala
XM_006718653.2:c.647T>C XP_006718716.1:p.Val216Ala
NM_053056.3:c.623T>C MANE Select NP_444284.1:p.Val208Ala