Canonical Allele Identifier: CA2792567603

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648215_69648216insACA , CM000673.2:g.69648215_69648216insACA	GRCh38
NC_000011.9:g.69462983_69462984insACA , CM000673.1:g.69462983_69462984insACA	GRCh37
NC_000011.8:g.69172164_69172165insACA	NCBI36
NG_007375.1:g.12111_12112insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+73_723+74insACA MANE Select	ENSP00000227507.2:n.723+73_723+74insACA
ENST00000227507.2:c.723+73_723+74insACA	ENSP00000227507.2:n.723+73_723+74insACA
ENST00000536559.1:c.*216_*217insACA	ENSP00000438482.1:n.*216_*217insACA
ENST00000542367.1:n.186+73_186+74insACA
NM_053056.2:c.723+73_723+74insACA	NP_444284.1:n.723+73_723+74insACA
XM_006718653.2:c.747+73_747+74insACA	XP_006718716.1:n.747+73_747+74insACA
NM_053056.3:c.723+73_723+74insACA MANE Select	NP_444284.1:n.723+73_723+74insACA