Canonical Allele Identifier: CA371162498
Gene: PRKDC HGNC NCBI

Linked Data

dbSNP Id: rs1454755701

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47862491A>C , CM000670.2:g.47862491A>C GRCh38
NC_000008.10:g.48775052A>C , CM000670.1:g.48775052A>C GRCh37
NC_000008.9:g.48937605A>C NCBI36
NG_023435.1:g.102693T>G , LRG_162:g.102693T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000314191.7:c.5801T>G MANE Select ENSP00000313420.3:p.Leu1934Arg
ENST00000314191.6:c.5801T>G ENSP00000313420.3:p.Leu1934Arg
ENST00000338368.7:c.5801T>G ENSP00000345182.4:p.Leu1934Arg
ENST00000546304.1:n.467T>G
NM_001081640.1:c.5801T>G NP_001075109.1:p.Leu1934Arg
NM_006904.6:c.5801T>G , LRG_162t1:c.5801T>G NP_008835.5:p.Leu1934Arg
XM_011517567.1:c.5801T>G XP_011515869.1:p.Leu1934Arg
XM_011517568.1:c.5801T>G XP_011515870.1:p.Leu1934Arg
NM_001081640.2:c.5801T>G NP_001075109.1:p.Leu1934Arg
NM_006904.7:c.5801T>G MANE Select NP_008835.5:p.Leu1934Arg