Canonical Allele Identifier: CA2579161019
Gene: PRKDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47789085G>T , CM000670.2:g.47789085G>T GRCh38
NC_000008.10:g.48701646G>T , CM000670.1:g.48701646G>T GRCh37
NC_000008.9:g.48864199G>T NCBI36
NG_023435.1:g.176099C>A , LRG_162:g.176099C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697602.1:n.1332-36C>A
ENST00000697603.1:c.3436-36C>A ENSP00000513358.1:n.3436-36C>A
ENST00000314191.7:c.10759-36C>A MANE Select ENSP00000313420.3:n.10759-36C>A
ENST00000314191.6:c.10759-36C>A ENSP00000313420.3:n.10759-36C>A
ENST00000338368.7:c.10759-36C>A ENSP00000345182.4:n.10759-36C>A
NM_001081640.1:c.10759-36C>A NP_001075109.1:n.10759-36C>A
NM_006904.6:c.10759-36C>A , LRG_162t1:c.10759-36C>A NP_008835.5:n.10759-36C>A
XM_011517567.1:c.10762-36C>A XP_011515869.1:n.10762-36C>A
XM_011517568.1:c.10762-36C>A XP_011515870.1:n.10762-36C>A
NM_001081640.2:c.10759-36C>A NP_001075109.1:n.10759-36C>A
NM_006904.7:c.10759-36C>A MANE Select NP_008835.5:n.10759-36C>A