Canonical Allele Identifier: CA581653075
Gene: PRKDC HGNC NCBI

Linked Data

dbSNP Id: rs1363364022

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47789059del , CM000670.2:g.47789059del GRCh38
NC_000008.10:g.48701620del , CM000670.1:g.48701620del GRCh37
NC_000008.9:g.48864173del NCBI36
NG_023435.1:g.176128del , LRG_162:g.176128del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697602.1:n.1332-7del
ENST00000697603.1:c.3436-7del ENSP00000513358.1:n.3436-7del
ENST00000314191.7:c.10759-7del MANE Select ENSP00000313420.3:n.10759-7del
ENST00000314191.6:c.10759-7del ENSP00000313420.3:n.10759-7del
ENST00000338368.7:c.10759-7del ENSP00000345182.4:n.10759-7del
NM_001081640.1:c.10759-7del NP_001075109.1:n.10759-7del
NM_006904.6:c.10759-7del , LRG_162t1:c.10759-7del NP_008835.5:n.10759-7del
XM_011517567.1:c.10762-7del XP_011515869.1:n.10762-7del
XM_011517568.1:c.10762-7del XP_011515870.1:n.10762-7del
NM_001081640.2:c.10759-7del NP_001075109.1:n.10759-7del
NM_006904.7:c.10759-7del MANE Select NP_008835.5:n.10759-7del