Canonical Allele Identifier: CA475219554

Gene: CCND1

Linked Data

• dbSNP Id: rs746640562
• MyVariant Identifiers: chr11:g.69462857C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648089C>T , CM000673.2:g.69648089C>T	GRCh38
NC_000011.9:g.69462857C>T , CM000673.1:g.69462857C>T	GRCh37
NC_000011.8:g.69172038C>T	NCBI36
NG_007375.1:g.11985C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.670C>T MANE Select	ENSP00000227507.2:p.Leu224=
ENST00000227507.2:c.670C>T	ENSP00000227507.2:p.Leu224=
ENST00000536559.1:c.*90C>T	ENSP00000438482.1:n.*90C>T
ENST00000542367.1:n.133C>T
ENST00000545484.1:n.376C>T
NM_053056.2:c.670C>T	NP_444284.1:p.Leu224=
XM_006718653.2:c.694C>T	XP_006718716.1:p.Leu232=
NM_053056.3:c.670C>T MANE Select	NP_444284.1:p.Leu224=