Canonical Allele Identifier: CA371162089

Gene: PRKDC

Linked Data

• MyVariant Identifiers: chr8:g.48774932A>C (hg19) ; chr8:g.47862371A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47862371A>C , CM000670.2:g.47862371A>C	GRCh38
NC_000008.10:g.48774932A>C , CM000670.1:g.48774932A>C	GRCh37
NC_000008.9:g.48937485A>C	NCBI36
NG_023435.1:g.102813T>G , LRG_162:g.102813T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000314191.7:c.5919+2T>G MANE Select	ENSP00000313420.3:n.5919+2T>G
ENST00000314191.6:c.5919+2T>G	ENSP00000313420.3:n.5919+2T>G
ENST00000338368.7:c.5919+2T>G	ENSP00000345182.4:n.5919+2T>G
ENST00000546304.1:n.587T>G
NM_001081640.1:c.5919+2T>G	NP_001075109.1:n.5919+2T>G
NM_006904.6:c.5919+2T>G , LRG_162t1:c.5919+2T>G	NP_008835.5:n.5919+2T>G
XM_011517567.1:c.5919+2T>G	XP_011515869.1:n.5919+2T>G
XM_011517568.1:c.5919+2T>G	XP_011515870.1:n.5919+2T>G
NM_001081640.2:c.5919+2T>G	NP_001075109.1:n.5919+2T>G
NM_006904.7:c.5919+2T>G MANE Select	NP_008835.5:n.5919+2T>G