Canonical Allele Identifier: CA1781875333
Community Standard Title: NM_006904.7(PRKDC):c.3464+326A=
Gene: PRKDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47898144T= , CM000670.2:g.47898144T= GRCh38
NC_000008.10:g.48810704T= , CM000670.1:g.48810704T= GRCh37
NC_000008.9:g.48973257T= NCBI36
NG_023435.1:g.67040A= , LRG_162:g.67040A=

Transcript Alleles

HGVS Amino-acid Change
NM_006904.7:c.3464+326A= MANE Select NP_008835.5:n.3464+326A=
ENST00000314191.7:c.3464+326A= MANE Select ENSP00000313420.3:n.3464+326A=
NM_001081640.1:c.3464+326A= NP_001075109.1:n.3464+326A=
NM_001081640.2:c.3464+326A= NP_001075109.1:n.3464+326A=
NM_006904.6:c.3464+326A= , LRG_162t1:c.3464+326A= NP_008835.5:n.3464+326A=
ENST00000314191.6:c.3464+326A= ENSP00000313420.3:n.3464+326A=
ENST00000338368.7:c.3464+326A= ENSP00000345182.4:n.3464+326A=
XM_011517567.1:c.3464+326A= XP_011515869.1:n.3464+326A=
XM_011517568.1:c.3464+326A= XP_011515870.1:n.3464+326A=