Canonical Allele Identifier: CA1781909118
Gene: PRKDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960136T= , CM000670.2:g.47960136T= GRCh38
NC_000008.10:g.48872696T= , CM000670.1:g.48872696T= GRCh37
NC_000008.9:g.49035249T= NCBI36
NG_023435.1:g.5048A= , LRG_162:g.5048A=
NG_032967.1:g.4934T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697591.1:n.32A=
ENST00000314191.7:c.-10A= MANE Select ENSP00000313420.3:n.-10A=
ENST00000314191.6:c.-10A= ENSP00000313420.3:n.-10A=
ENST00000338368.7:c.-10A= ENSP00000345182.4:n.-10A=
NM_001081640.1:c.-10A= NP_001075109.1:n.-10A=
NM_006904.6:c.-10A= , LRG_162t1:c.-10A= NP_008835.5:n.-10A=
XM_011517567.1:c.-10A= XP_011515869.1:n.-10A=
XM_011517568.1:c.-10A= XP_011515870.1:n.-10A=
NM_001081640.2:c.-10A= NP_001075109.1:n.-10A=
NM_006904.7:c.-10A= MANE Select NP_008835.5:n.-10A=