Canonical Allele Identifier: CA381658025
Gene: CCND1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648044G>T , CM000673.2:g.69648044G>T GRCh38
NC_000011.9:g.69462812G>T , CM000673.1:g.69462812G>T GRCh37
NC_000011.8:g.69171993G>T NCBI36
NG_007375.1:g.11940G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.625G>T MANE Select ENSP00000227507.2:p.Val209Leu
ENST00000227507.2:c.625G>T ENSP00000227507.2:p.Val209Leu
ENST00000536559.1:c.*45G>T ENSP00000438482.1:n.*45G>T
ENST00000542367.1:n.88G>T
ENST00000545484.1:n.331G>T
NM_053056.2:c.625G>T NP_444284.1:p.Val209Leu
XM_006718653.2:c.649G>T XP_006718716.1:p.Val217Leu
NM_053056.3:c.625G>T MANE Select NP_444284.1:p.Val209Leu