Canonical Allele Identifier: CA381658021
Gene: CCND1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.623T>G MANE Select ENSP00000227507.2:p.Val208Gly
ENST00000227507.2:c.623T>G ENSP00000227507.2:p.Val208Gly
ENST00000536559.1:c.*43T>G ENSP00000438482.1:n.*43T>G
ENST00000542367.1:n.86T>G
ENST00000545484.1:n.329T>G
NM_053056.2:c.623T>G NP_444284.1:p.Val208Gly
XM_006718653.2:c.647T>G XP_006718716.1:p.Val216Gly
NM_053056.3:c.623T>G MANE Select NP_444284.1:p.Val208Gly