Canonical Allele Identifier: CA460603960

Gene: PRKDC

Linked Data

• gnomAD v4: 8-47789151-C-T
• MyVariant Identifiers: chr8:g.48701712C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47789151C>T , CM000670.2:g.47789151C>T	GRCh38
NC_000008.10:g.48701712C>T , CM000670.1:g.48701712C>T	GRCh37
NC_000008.9:g.48864265C>T	NCBI36
NG_023435.1:g.176033G>A , LRG_162:g.176033G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697602.1:n.1331G>A
ENST00000697603.1:c.3435G>A	ENSP00000513358.1:p.Lys1145=
ENST00000314191.7:c.10758G>A MANE Select	ENSP00000313420.3:p.Lys3586=
ENST00000314191.6:c.10758G>A	ENSP00000313420.3:p.Lys3586=
ENST00000338368.7:c.10758G>A	ENSP00000345182.4:p.Lys3586=
NM_001081640.1:c.10758G>A	NP_001075109.1:p.Lys3586=
NM_006904.6:c.10758G>A , LRG_162t1:c.10758G>A	NP_008835.5:p.Lys3586=
XM_011517567.1:c.10761G>A	XP_011515869.1:p.Lys3587=
XM_011517568.1:c.10761G>A	XP_011515870.1:p.Lys3587=
NM_001081640.2:c.10758G>A	NP_001075109.1:p.Lys3586=
NM_006904.7:c.10758G>A MANE Select	NP_008835.5:p.Lys3586=