Canonical Allele Identifier: CA2830782912

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648133_69648142delinsATGTGACCCA , CM000673.2:g.69648133_69648142delinsATGTGACCCA	GRCh38
NC_000011.9:g.69462901_69462910delinsATGTGACCCA , CM000673.1:g.69462901_69462910delinsATGTGACCCA	GRCh37
NC_000011.8:g.69172082_69172091delinsATGTGACCCA	NCBI36
NG_007375.1:g.12029_12038delinsATGTGACCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.714_723delinsATGTGACCCA MANE Select	ENSP00000227507.2:p.Lys238=
ENST00000227507.2:c.714_723delinsATGTGACCCA	ENSP00000227507.2:p.Lys238=
ENST00000536559.1:c.*134_*143delinsATGTGACCCA	ENSP00000438482.1:n.*134_*143delinsATGTGACCCA
ENST00000542367.1:n.177_186delinsATGTGACCCA
ENST00000545484.1:n.420_429delinsATGTGACCCA
NM_053056.2:c.714_723delinsATGTGACCCA	NP_444284.1:p.Lys238=
XM_006718653.2:c.738_747delinsATGTGACCCA	XP_006718716.1:p.Lys246=
NM_053056.3:c.714_723delinsATGTGACCCA MANE Select	NP_444284.1:p.Lys238=