Canonical Allele Identifier: CA460606239

Gene: PRKDC

Linked Data

• dbSNP Id: rs1229174262
• gnomAD v4: 8-47852766-C-T
• MyVariant Identifiers: chr8:g.48765327C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47852766C>T , CM000670.2:g.47852766C>T	GRCh38
NC_000008.10:g.48765327C>T , CM000670.1:g.48765327C>T	GRCh37
NC_000008.9:g.48927880C>T	NCBI36
NG_023435.1:g.112418G>A , LRG_162:g.112418G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000314191.7:c.6912G>A MANE Select	ENSP00000313420.3:p.Val2304=
ENST00000314191.6:c.6912G>A	ENSP00000313420.3:p.Val2304=
ENST00000338368.7:c.6912G>A	ENSP00000345182.4:p.Val2304=
NM_001081640.1:c.6912G>A	NP_001075109.1:p.Val2304=
NM_006904.6:c.6912G>A , LRG_162t1:c.6912G>A	NP_008835.5:p.Val2304=
XM_011517567.1:c.6912G>A	XP_011515869.1:p.Val2304=
XM_011517568.1:c.6912G>A	XP_011515870.1:p.Val2304=
NM_001081640.2:c.6912G>A	NP_001075109.1:p.Val2304=
NM_006904.7:c.6912G>A MANE Select	NP_008835.5:p.Val2304=