Canonical Allele Identifier: CA2792567608

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648220_69648221insA , CM000673.2:g.69648220_69648221insA	GRCh38
NC_000011.9:g.69462988_69462989insA , CM000673.1:g.69462988_69462989insA	GRCh37
NC_000011.8:g.69172169_69172170insA	NCBI36
NG_007375.1:g.12116_12117insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+78_723+79insA MANE Select	ENSP00000227507.2:n.723+78_723+79insA
ENST00000227507.2:c.723+78_723+79insA	ENSP00000227507.2:n.723+78_723+79insA
ENST00000536559.1:c.*221_*222insA	ENSP00000438482.1:n.*221_*222insA
ENST00000542367.1:n.186+78_186+79insA
NM_053056.2:c.723+78_723+79insA	NP_444284.1:n.723+78_723+79insA
XM_006718653.2:c.747+78_747+79insA	XP_006718716.1:n.747+78_747+79insA
NM_053056.3:c.723+78_723+79insA MANE Select	NP_444284.1:n.723+78_723+79insA