Canonical Allele Identifier: CA381657920

Gene: CCND1

Linked Data

• MyVariant Identifiers: chr11:g.69462765T>A (hg19) ; chr11:g.69647997T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69647997T>A , CM000673.2:g.69647997T>A	GRCh38
NC_000011.9:g.69462765T>A , CM000673.1:g.69462765T>A	GRCh37
NC_000011.8:g.69171946T>A	NCBI36
NG_007375.1:g.11893T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.578T>A MANE Select	ENSP00000227507.2:p.Val193Glu
ENST00000227507.2:c.578T>A	ENSP00000227507.2:p.Val193Glu
ENST00000536559.1:c.202T>A	ENSP00000438482.1:p.Ter68Arg
ENST00000542367.1:n.41T>A
ENST00000545484.1:n.284T>A
NM_053056.2:c.578T>A	NP_444284.1:p.Val193Glu
XM_006718653.2:c.602T>A	XP_006718716.1:p.Val201Glu
NM_053056.3:c.578T>A MANE Select	NP_444284.1:p.Val193Glu