Canonical Allele Identifier: CA381658022
Gene: CCND1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.623T>A MANE Select ENSP00000227507.2:p.Val208Glu
ENST00000227507.2:c.623T>A ENSP00000227507.2:p.Val208Glu
ENST00000536559.1:c.*43T>A ENSP00000438482.1:n.*43T>A
ENST00000542367.1:n.86T>A
ENST00000545484.1:n.329T>A
NM_053056.2:c.623T>A NP_444284.1:p.Val208Glu
XM_006718653.2:c.647T>A XP_006718716.1:p.Val216Glu
NM_053056.3:c.623T>A MANE Select NP_444284.1:p.Val208Glu