Canonical Allele Identifier: CA3804155

Gene: CCND3

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372991.9:c.759G>T MANE Select	ENSP00000362082.5:p.Glu253Asp
ENST00000372987.8:c.609G>T	ENSP00000362078.4:p.Glu203Asp
ENST00000372988.8:c.516G>T	ENSP00000362079.4:p.Glu172Asp
ENST00000372991.8:c.759G>T	ENSP00000362082.4:p.Glu253Asp
ENST00000414200.6:c.543G>T	ENSP00000397545.2:p.Glu181Asp
ENST00000415497.6:c.171G>T	ENSP00000401595.2:p.Glu57Asp
ENST00000510503.5:c.379G>T	ENSP00000425986.1:p.Glu127Ter
ENST00000511642.5:c.516G>T	ENSP00000426212.1:p.Glu172Asp
ENST00000511686.5:n.412G>T
ENST00000616010.4:c.171G>T	ENSP00000484424.1:p.Glu57Asp
NM_001136017.3:c.516G>T	NP_001129489.1:p.Glu172Asp
NM_001136125.2:c.543G>T	NP_001129597.1:p.Glu181Asp
NM_001136126.2:c.171G>T	NP_001129598.1:p.Glu57Asp
NM_001287427.1:c.609G>T	NP_001274356.1:p.Glu203Asp
NM_001287434.1:c.171G>T	NP_001274363.1:p.Glu57Asp
NM_001760.4:c.759G>T	NP_001751.1:p.Glu253Asp
XM_011514971.1:c.622G>T	XP_011513273.1:p.Glu208Ter
XM_011514972.1:c.379G>T	XP_011513274.1:p.Glu127Ter
XM_011514971.2:c.622G>T	XP_011513273.1:p.Glu208Ter
NM_001760.5:c.759G>T MANE Select	NP_001751.1:p.Glu253Asp
NM_001136125.3:c.543G>T	NP_001129597.1:p.Glu181Asp
NM_001136126.3:c.171G>T	NP_001129598.1:p.Glu57Asp
NM_001287427.2:c.609G>T	NP_001274356.1:p.Glu203Asp
NM_001287434.2:c.171G>T	NP_001274363.1:p.Glu57Asp