Canonical Allele Identifier: CA2792567612

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648226_69648227insA , CM000673.2:g.69648226_69648227insA	GRCh38
NC_000011.9:g.69462994_69462995insA , CM000673.1:g.69462994_69462995insA	GRCh37
NC_000011.8:g.69172175_69172176insA	NCBI36
NG_007375.1:g.12122_12123insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+84_723+85insA MANE Select	ENSP00000227507.2:n.723+84_723+85insA
ENST00000227507.2:c.723+84_723+85insA	ENSP00000227507.2:n.723+84_723+85insA
ENST00000536559.1:c.*227_*228insA	ENSP00000438482.1:n.*227_*228insA
ENST00000542367.1:n.186+84_186+85insA
NM_053056.2:c.723+84_723+85insA	NP_444284.1:n.723+84_723+85insA
XM_006718653.2:c.747+84_747+85insA	XP_006718716.1:n.747+84_747+85insA
NM_053056.3:c.723+84_723+85insA MANE Select	NP_444284.1:n.723+84_723+85insA