Canonical Allele Identifier: CA2670075798
Gene: CC2D2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15559165del , CM000666.2:g.15559165del GRCh38
NC_000004.11:g.15560788del , CM000666.1:g.15560788del GRCh37
NC_000004.10:g.15169886del NCBI36
NG_013035.1:g.94300del , LRG_697:g.94300del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389652.11:c.2830del
ENST00000424120.6:c.2830del
ENST00000503292.6:c.2830del
ENST00000506643.5:c.2683del
ENST00000634028.2:c.2683del
ENST00000650860.2:c.2683del
ENST00000674945.1:c.2683del
ENST00000675619.1:n.909del
ENST00000675768.1:n.50del
ENST00000676337.1:c.2683del
ENST00000680586.1:n.757del
ENST00000389652.9:c.2292del
ENST00000424120.5:c.2830del
ENST00000503292.5:c.2830del
ENST00000506643.4:c.1158del
ENST00000634028.1:c.2813del
NM_001080522.2:c.2830del , LRG_697t1:c.2830del
XM_005248177.1:c.2830del
XM_011513869.1:c.2830del
XM_011513870.1:c.2830del
XM_011513871.1:c.2683del
XM_011513872.1:c.2830del
XM_011513873.1:c.2830del
XM_011513872.3:c.2830del
XM_017008482.1:c.2683del
XR_001741296.1:n.3030del
NM_001378615.1:c.2830del
NM_001378617.1:c.2683del