Canonical Allele Identifier: CA475219580

Gene: CCND1

Linked Data

• dbSNP Id: rs2120110041
• MyVariant Identifiers: chr11:g.69462892A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648124A>G , CM000673.2:g.69648124A>G	GRCh38
NC_000011.9:g.69462892A>G , CM000673.1:g.69462892A>G	GRCh37
NC_000011.8:g.69172073A>G	NCBI36
NG_007375.1:g.12020A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.705A>G MANE Select	ENSP00000227507.2:p.Arg235=
ENST00000227507.2:c.705A>G	ENSP00000227507.2:p.Arg235=
ENST00000536559.1:c.*125A>G	ENSP00000438482.1:n.*125A>G
ENST00000542367.1:n.168A>G
ENST00000545484.1:n.411A>G
NM_053056.2:c.705A>G	NP_444284.1:p.Arg235=
XM_006718653.2:c.729A>G	XP_006718716.1:p.Arg243=
NM_053056.3:c.705A>G MANE Select	NP_444284.1:p.Arg235=