Canonical Allele Identifier: CA2497327835

Gene: CCND1

Linked Data

• dbSNP Id: rs1855801706

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69647723del , CM000673.2:g.69647723del	GRCh38
NC_000011.9:g.69462491del , CM000673.1:g.69462491del	GRCh37
NC_000011.8:g.69171672del	NCBI36
NG_007375.1:g.11619del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.575-271del MANE Select	ENSP00000227507.2:n.575-271del
ENST00000227507.2:c.575-271del	ENSP00000227507.2:n.575-271del
ENST00000536559.1:c.199-271del	ENSP00000438482.1:n.199-271del
ENST00000545484.1:n.281-271del
NM_053056.2:c.575-271del	NP_444284.1:n.575-271del
XM_006718653.2:c.599-271del	XP_006718716.1:n.599-271del
NM_053056.3:c.575-271del MANE Select	NP_444284.1:n.575-271del