Canonical Allele Identifier: CA1623826249

Gene: CCND3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41936060C= , CM000668.2:g.41936060C=	GRCh38
NC_000006.11:g.41903798C= , CM000668.1:g.41903798C=	GRCh37
NC_000006.10:g.42011776C=	NCBI36
NG_041939.1:g.117835G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001760.5:c.759G= MANE Select	NP_001751.1:p.Glu253=
ENST00000372991.9:c.759G= MANE Select	ENSP00000362082.5:p.Glu253=
NM_001136017.3:c.516G=	NP_001129489.1:p.Glu172=
NM_001136125.2:c.543G=	NP_001129597.1:p.Glu181=
NM_001136125.3:c.543G=	NP_001129597.1:p.Glu181=
NM_001136126.2:c.171G=	NP_001129598.1:p.Glu57=
NM_001136126.3:c.171G=	NP_001129598.1:p.Glu57=
NM_001287427.1:c.609G=	NP_001274356.1:p.Glu203=
NM_001287427.2:c.609G=	NP_001274356.1:p.Glu203=
NM_001287434.1:c.171G=	NP_001274363.1:p.Glu57=
NM_001287434.2:c.171G=	NP_001274363.1:p.Glu57=
NM_001760.4:c.759G=	NP_001751.1:p.Glu253=
ENST00000372987.8:c.609G=	ENSP00000362078.4:p.Glu203=
ENST00000372988.8:c.516G=	ENSP00000362079.4:p.Glu172=
ENST00000372991.8:c.759G=	ENSP00000362082.4:p.Glu253=
ENST00000414200.6:c.543G=	ENSP00000397545.2:p.Glu181=
ENST00000415497.6:c.171G=	ENSP00000401595.2:p.Glu57=
ENST00000510503.5:c.379G=	ENSP00000425986.1:p.Glu127=
ENST00000511642.5:c.516G=	ENSP00000426212.1:p.Glu172=
ENST00000511686.5:n.412G=
ENST00000616010.4:c.171G=	ENSP00000484424.1:p.Glu57=
XM_011514971.1:c.622G=	XP_011513273.1:p.Glu208=
XM_011514971.2:c.622G=	XP_011513273.1:p.Glu208=
XM_011514972.1:c.379G=	XP_011513274.1:p.Glu127=