Canonical Allele Identifier: CA2792567596

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648197_69648198insACT , CM000673.2:g.69648197_69648198insACT	GRCh38
NC_000011.9:g.69462965_69462966insACT , CM000673.1:g.69462965_69462966insACT	GRCh37
NC_000011.8:g.69172146_69172147insACT	NCBI36
NG_007375.1:g.12093_12094insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+55_723+56insACT MANE Select	ENSP00000227507.2:n.723+55_723+56insACT
ENST00000227507.2:c.723+55_723+56insACT	ENSP00000227507.2:n.723+55_723+56insACT
ENST00000536559.1:c.*198_*199insACT	ENSP00000438482.1:n.*198_*199insACT
ENST00000542367.1:n.186+55_186+56insACT
NM_053056.2:c.723+55_723+56insACT	NP_444284.1:n.723+55_723+56insACT
XM_006718653.2:c.747+55_747+56insACT	XP_006718716.1:n.747+55_747+56insACT
NM_053056.3:c.723+55_723+56insACT MANE Select	NP_444284.1:n.723+55_723+56insACT