Canonical Allele Identifier: CA16263020

Gene: CCND3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41946640A>G , CM000668.2:g.41946640A>G	GRCh38
NC_000006.11:g.41914378A>G , CM000668.1:g.41914378A>G	GRCh37
NC_000006.10:g.42022356A>G	NCBI36
NG_041939.1:g.107255T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001136017.3:c.-45-6055T>C	NP_001129489.1:n.-45-6055T>C
NM_001136126.2:c.-174-9246T>C	NP_001129598.1:n.-174-9246T>C
NM_001136126.3:c.-174-9246T>C	NP_001129598.1:n.-174-9246T>C
NM_001287434.1:c.-174-9246T>C	NP_001274363.1:n.-174-9246T>C
NM_001287434.2:c.-174-9246T>C	NP_001274363.1:n.-174-9246T>C
ENST00000372988.8:c.-45-6055T>C	ENSP00000362079.4:n.-45-6055T>C
ENST00000415497.6:c.-174-9246T>C	ENSP00000401595.2:n.-174-9246T>C
ENST00000502771.1:c.-45-6055T>C	ENSP00000425334.1:n.-45-6055T>C
ENST00000505672.5:n.177-6055T>C
ENST00000505884.5:n.373-9246T>C
ENST00000508143.5:c.-174-9246T>C	ENSP00000423242.1:n.-174-9246T>C
ENST00000510503.5:c.-45-6055T>C	ENSP00000425986.1:n.-45-6055T>C
ENST00000511161.5:n.191-9246T>C
ENST00000511642.5:c.-45-6055T>C	ENSP00000426212.1:n.-45-6055T>C
ENST00000511686.5:n.205-9246T>C
ENST00000513956.5:n.191-9246T>C
ENST00000514382.5:n.189-6055T>C
ENST00000514588.1:c.-162-5479T>C	ENSP00000420991.1:n.-162-5479T>C
ENST00000616010.4:c.-174-9246T>C	ENSP00000484424.1:n.-174-9246T>C
XM_011514972.1:c.-45-6055T>C	XP_011513274.1:n.-45-6055T>C