Canonical Allele Identifier: CA371132311

Gene: PRKDC

Linked Data

• gnomAD v4: 8-47789048-T-A
• MyVariant Identifiers: chr8:g.48701609T>A (hg19) ; chr8:g.47789048T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47789048T>A , CM000670.2:g.47789048T>A	GRCh38
NC_000008.10:g.48701609T>A , CM000670.1:g.48701609T>A	GRCh37
NC_000008.9:g.48864162T>A	NCBI36
NG_023435.1:g.176136A>T , LRG_162:g.176136A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697602.1:n.1333A>T
ENST00000697603.1:c.3437A>T	ENSP00000513358.1:p.Asp1146Val
ENST00000314191.7:c.10760A>T MANE Select	ENSP00000313420.3:p.Asp3587Val
ENST00000314191.6:c.10760A>T	ENSP00000313420.3:p.Asp3587Val
ENST00000338368.7:c.10760A>T	ENSP00000345182.4:p.Asp3587Val
NM_001081640.1:c.10760A>T	NP_001075109.1:p.Asp3587Val
NM_006904.6:c.10760A>T , LRG_162t1:c.10760A>T	NP_008835.5:p.Asp3587Val
XM_011517567.1:c.10763A>T	XP_011515869.1:p.Asp3588Val
XM_011517568.1:c.10763A>T	XP_011515870.1:p.Asp3588Val
NM_001081640.2:c.10760A>T	NP_001075109.1:p.Asp3587Val
NM_006904.7:c.10760A>T MANE Select	NP_008835.5:p.Asp3587Val