Canonical Allele Identifier: CA1781813557
Gene: PRKDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47789075A= , CM000670.2:g.47789075A= GRCh38
NC_000008.10:g.48701636A= , CM000670.1:g.48701636A= GRCh37
NC_000008.9:g.48864189A= NCBI36
NG_023435.1:g.176109T= , LRG_162:g.176109T=

Transcript Alleles

HGVS Amino-acid change
ENST00000697602.1:n.1332-26T=
ENST00000697603.1:c.3436-26T= ENSP00000513358.1:n.3436-26T=
ENST00000314191.7:c.10759-26T= MANE Select ENSP00000313420.3:n.10759-26T=
ENST00000314191.6:c.10759-26T= ENSP00000313420.3:n.10759-26T=
ENST00000338368.7:c.10759-26T= ENSP00000345182.4:n.10759-26T=
NM_001081640.1:c.10759-26T= NP_001075109.1:n.10759-26T=
NM_006904.6:c.10759-26T= , LRG_162t1:c.10759-26T= NP_008835.5:n.10759-26T=
XM_011517567.1:c.10762-26T= XP_011515869.1:n.10762-26T=
XM_011517568.1:c.10762-26T= XP_011515870.1:n.10762-26T=
NM_001081640.2:c.10759-26T= NP_001075109.1:n.10759-26T=
NM_006904.7:c.10759-26T= MANE Select NP_008835.5:n.10759-26T=