Canonical Allele Identifier: CA1781813558

Gene: PRKDC

Linked Data

• dbSNP Id: rs2086841030
• gnomAD v4: 8-47789075-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47789075A>G , CM000670.2:g.47789075A>G	GRCh38
NC_000008.10:g.48701636A>G , CM000670.1:g.48701636A>G	GRCh37
NC_000008.9:g.48864189A>G	NCBI36
NG_023435.1:g.176109T>C , LRG_162:g.176109T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697602.1:n.1332-26T>C
ENST00000697603.1:c.3436-26T>C	ENSP00000513358.1:n.3436-26T>C
ENST00000314191.7:c.10759-26T>C MANE Select	ENSP00000313420.3:n.10759-26T>C
ENST00000314191.6:c.10759-26T>C	ENSP00000313420.3:n.10759-26T>C
ENST00000338368.7:c.10759-26T>C	ENSP00000345182.4:n.10759-26T>C
NM_001081640.1:c.10759-26T>C	NP_001075109.1:n.10759-26T>C
NM_006904.6:c.10759-26T>C , LRG_162t1:c.10759-26T>C	NP_008835.5:n.10759-26T>C
XM_011517567.1:c.10762-26T>C	XP_011515869.1:n.10762-26T>C
XM_011517568.1:c.10762-26T>C	XP_011515870.1:n.10762-26T>C
NM_001081640.2:c.10759-26T>C	NP_001075109.1:n.10759-26T>C
NM_006904.7:c.10759-26T>C MANE Select	NP_008835.5:n.10759-26T>C