Canonical Allele Identifier: CA475219573

Gene: CCND1

Linked Data

• MyVariant Identifiers: chr11:g.69462886C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648118C>A , CM000673.2:g.69648118C>A	GRCh38
NC_000011.9:g.69462886C>A , CM000673.1:g.69462886C>A	GRCh37
NC_000011.8:g.69172067C>A	NCBI36
NG_007375.1:g.12014C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.699C>A MANE Select	ENSP00000227507.2:p.Leu233=
ENST00000227507.2:c.699C>A	ENSP00000227507.2:p.Leu233=
ENST00000536559.1:c.*119C>A	ENSP00000438482.1:n.*119C>A
ENST00000542367.1:n.162C>A
ENST00000545484.1:n.405C>A
NM_053056.2:c.699C>A	NP_444284.1:p.Leu233=
XM_006718653.2:c.723C>A	XP_006718716.1:p.Leu241=
NM_053056.3:c.699C>A MANE Select	NP_444284.1:p.Leu233=