Canonical Allele Identifier: CA4741079
Community Standard Title: NM_006904.7(PRKDC):c.3834G>A (p.Ala1278=)
Gene: PRKDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47893152C>T , CM000670.2:g.47893152C>T GRCh38
NC_000008.10:g.48805713C>T , CM000670.1:g.48805713C>T GRCh37
NC_000008.9:g.48968266C>T NCBI36
NG_023435.1:g.72032G>A , LRG_162:g.72032G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006904.7:c.3834G>A MANE Select NP_008835.5:p.Ala1278=
ENST00000314191.7:c.3834G>A MANE Select ENSP00000313420.3:p.Ala1278=
NM_001081640.1:c.3834G>A NP_001075109.1:p.Ala1278=
NM_001081640.2:c.3834G>A NP_001075109.1:p.Ala1278=
NM_006904.6:c.3834G>A , LRG_162t1:c.3834G>A NP_008835.5:p.Ala1278=
ENST00000314191.6:c.3834G>A ENSP00000313420.3:p.Ala1278=
ENST00000338368.7:c.3834G>A ENSP00000345182.4:p.Ala1278=
XM_011517567.1:c.3834G>A XP_011515869.1:p.Ala1278=
XM_011517568.1:c.3834G>A XP_011515870.1:p.Ala1278=