Canonical Allele Identifier: CA1781838151
Gene: PRKDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47817443G= , CM000670.2:g.47817443G= GRCh38
NC_000008.10:g.48730004G= , CM000670.1:g.48730004G= GRCh37
NC_000008.9:g.48892557G= NCBI36
NG_023435.1:g.147741C= , LRG_162:g.147741C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697603.1:c.2234+7C= ENSP00000513358.1:n.2234+7C=
ENST00000697607.1:n.1089+7C=
ENST00000314191.7:c.9557+7C= MANE Select ENSP00000313420.3:n.9557+7C=
ENST00000314191.6:c.9557+7C= ENSP00000313420.3:n.9557+7C=
ENST00000338368.7:c.9557+7C= ENSP00000345182.4:n.9557+7C=
NM_001081640.1:c.9557+7C= NP_001075109.1:n.9557+7C=
NM_006904.6:c.9557+7C= , LRG_162t1:c.9557+7C= NP_008835.5:n.9557+7C=
XM_011517567.1:c.9560+7C= XP_011515869.1:n.9560+7C=
XM_011517568.1:c.9560+7C= XP_011515870.1:n.9560+7C=
NM_001081640.2:c.9557+7C= NP_001075109.1:n.9557+7C=
NM_006904.7:c.9557+7C= MANE Select NP_008835.5:n.9557+7C=