Canonical Allele Identifier: CA2792567595

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648197_69648198insA , CM000673.2:g.69648197_69648198insA	GRCh38
NC_000011.9:g.69462965_69462966insA , CM000673.1:g.69462965_69462966insA	GRCh37
NC_000011.8:g.69172146_69172147insA	NCBI36
NG_007375.1:g.12093_12094insA

Transcript Alleles

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