Canonical Allele Identifier: CA2614780104

Gene: CCND1

Linked Data

• gnomAD v4: 11-69648275-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648279del , CM000673.2:g.69648279del	GRCh38
NC_000011.9:g.69463047del , CM000673.1:g.69463047del	GRCh37
NC_000011.8:g.69172228del	NCBI36
NG_007375.1:g.12175del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+137del MANE Select	ENSP00000227507.2:n.723+137del
ENST00000227507.2:c.723+137del	ENSP00000227507.2:n.723+137del
ENST00000542367.1:n.186+137del
NM_053056.2:c.723+137del	NP_444284.1:n.723+137del
XM_006718653.2:c.747+137del	XP_006718716.1:n.747+137del
NM_053056.3:c.723+137del MANE Select	NP_444284.1:n.723+137del