Canonical Allele Identifier: CA1781813559
Gene: PRKDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47789091T= , CM000670.2:g.47789091T= GRCh38
NC_000008.10:g.48701652T= , CM000670.1:g.48701652T= GRCh37
NC_000008.9:g.48864205T= NCBI36
NG_023435.1:g.176093A= , LRG_162:g.176093A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697602.1:n.1332-42A=
ENST00000697603.1:c.3436-42A= ENSP00000513358.1:n.3436-42A=
ENST00000314191.7:c.10759-42A= MANE Select ENSP00000313420.3:n.10759-42A=
ENST00000314191.6:c.10759-42A= ENSP00000313420.3:n.10759-42A=
ENST00000338368.7:c.10759-42A= ENSP00000345182.4:n.10759-42A=
NM_001081640.1:c.10759-42A= NP_001075109.1:n.10759-42A=
NM_006904.6:c.10759-42A= , LRG_162t1:c.10759-42A= NP_008835.5:n.10759-42A=
XM_011517567.1:c.10762-42A= XP_011515869.1:n.10762-42A=
XM_011517568.1:c.10762-42A= XP_011515870.1:n.10762-42A=
NM_001081640.2:c.10759-42A= NP_001075109.1:n.10759-42A=
NM_006904.7:c.10759-42A= MANE Select NP_008835.5:n.10759-42A=