Canonical Allele Identifier: CA381658189

Gene: CCND1

Linked Data

• MyVariant Identifiers: chr11:g.69462891G>T (hg19) ; chr11:g.69648123G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648123G>T , CM000673.2:g.69648123G>T	GRCh38
NC_000011.9:g.69462891G>T , CM000673.1:g.69462891G>T	GRCh37
NC_000011.8:g.69172072G>T	NCBI36
NG_007375.1:g.12019G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.704G>T MANE Select	ENSP00000227507.2:p.Arg235Ile
ENST00000227507.2:c.704G>T	ENSP00000227507.2:p.Arg235Ile
ENST00000536559.1:c.*124G>T	ENSP00000438482.1:n.*124G>T
ENST00000542367.1:n.167G>T
ENST00000545484.1:n.410G>T
NM_053056.2:c.704G>T	NP_444284.1:p.Arg235Ile
XM_006718653.2:c.728G>T	XP_006718716.1:p.Arg243Ile
NM_053056.3:c.704G>T MANE Select	NP_444284.1:p.Arg235Ile