Canonical Allele Identifier: CA1781813587
Gene: PRKDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47789138G= , CM000670.2:g.47789138G= GRCh38
NC_000008.10:g.48701699G= , CM000670.1:g.48701699G= GRCh37
NC_000008.9:g.48864252G= NCBI36
NG_023435.1:g.176046C= , LRG_162:g.176046C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697602.1:n.1331+13C=
ENST00000697603.1:c.3435+13C= ENSP00000513358.1:n.3435+13C=
ENST00000314191.7:c.10758+13C= MANE Select ENSP00000313420.3:n.10758+13C=
ENST00000314191.6:c.10758+13C= ENSP00000313420.3:n.10758+13C=
ENST00000338368.7:c.10758+13C= ENSP00000345182.4:n.10758+13C=
NM_001081640.1:c.10758+13C= NP_001075109.1:n.10758+13C=
NM_006904.6:c.10758+13C= , LRG_162t1:c.10758+13C= NP_008835.5:n.10758+13C=
XM_011517567.1:c.10761+13C= XP_011515869.1:n.10761+13C=
XM_011517568.1:c.10761+13C= XP_011515870.1:n.10761+13C=
NM_001081640.2:c.10758+13C= NP_001075109.1:n.10758+13C=
NM_006904.7:c.10758+13C= MANE Select NP_008835.5:n.10758+13C=