Canonical Allele Identifier: CA2792567593

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648192_69648198del , CM000673.2:g.69648192_69648198del	GRCh38
NC_000011.9:g.69462960_69462966del , CM000673.1:g.69462960_69462966del	GRCh37
NC_000011.8:g.69172141_69172147del	NCBI36
NG_007375.1:g.12088_12094del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+50_723+56del MANE Select	ENSP00000227507.2:n.723+50_723+56del
ENST00000227507.2:c.723+50_723+56del	ENSP00000227507.2:n.723+50_723+56del
ENST00000536559.1:c.*193_*199del	ENSP00000438482.1:n.*193_*199del
ENST00000542367.1:n.186+50_186+56del
NM_053056.2:c.723+50_723+56del	NP_444284.1:n.723+50_723+56del
XM_006718653.2:c.747+50_747+56del	XP_006718716.1:n.747+50_747+56del
NM_053056.3:c.723+50_723+56del MANE Select	NP_444284.1:n.723+50_723+56del