Canonical Allele Identifier: CA2792567606

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648219_69648220insACA , CM000673.2:g.69648219_69648220insACA	GRCh38
NC_000011.9:g.69462987_69462988insACA , CM000673.1:g.69462987_69462988insACA	GRCh37
NC_000011.8:g.69172168_69172169insACA	NCBI36
NG_007375.1:g.12115_12116insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+77_723+78insACA MANE Select	ENSP00000227507.2:n.723+77_723+78insACA
ENST00000227507.2:c.723+77_723+78insACA	ENSP00000227507.2:n.723+77_723+78insACA
ENST00000536559.1:c.*220_*221insACA	ENSP00000438482.1:n.*220_*221insACA
ENST00000542367.1:n.186+77_186+78insACA
NM_053056.2:c.723+77_723+78insACA	NP_444284.1:n.723+77_723+78insACA
XM_006718653.2:c.747+77_747+78insACA	XP_006718716.1:n.747+77_747+78insACA
NM_053056.3:c.723+77_723+78insACA MANE Select	NP_444284.1:n.723+77_723+78insACA