Canonical Allele Identifier: CA2670075797
Gene: CC2D2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15559163_15559166del , CM000666.2:g.15559163_15559166del GRCh38
NC_000004.11:g.15560786_15560789del , CM000666.1:g.15560786_15560789del GRCh37
NC_000004.10:g.15169884_15169887del NCBI36
NG_013035.1:g.94298_94301del , LRG_697:g.94298_94301del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389652.11:c.2830-2_2831del
ENST00000424120.6:c.2830-2_2831del
ENST00000503292.6:c.2830-2_2831del
ENST00000506643.5:c.2683-2_2684del
ENST00000634028.2:c.2683-2_2684del
ENST00000650860.2:c.2683-2_2684del
ENST00000674945.1:c.2683-2_2684del
ENST00000675619.1:n.909-2_910del
ENST00000675768.1:n.50-2_51del
ENST00000676337.1:c.2683-2_2684del
ENST00000680586.1:n.757-2_758del
ENST00000389652.9:c.2292-2_2293del
ENST00000424120.5:c.2830-2_2831del
ENST00000503292.5:c.2830-2_2831del
ENST00000506643.4:c.1158-2_1159del
ENST00000634028.1:c.2813-2_2814del
NM_001080522.2:c.2830-2_2831del , LRG_697t1:c.2830-2_2831del
XM_005248177.1:c.2830-2_2831del
XM_011513869.1:c.2830-2_2831del
XM_011513870.1:c.2830-2_2831del
XM_011513871.1:c.2683-2_2684del
XM_011513872.1:c.2830-2_2831del
XM_011513873.1:c.2830-2_2831del
XM_011513872.3:c.2830-2_2831del
XM_017008482.1:c.2683-2_2684del
XR_001741296.1:n.3030-2_3031del
NM_001378615.1:c.2830-2_2831del
NM_001378617.1:c.2683-2_2684del