Canonical Allele Identifier: CA176162012

Gene: PRKDC

Linked Data

• dbSNP Id: rs964939079
• MyVariant Identifiers: chr8:g.47920332G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47920332G>A , CM000670.2:g.47920332G>A	GRCh38
NC_000008.10:g.48832892G>A , CM000670.1:g.48832892G>A	GRCh37
NC_000008.9:g.48995445G>A	NCBI36
NG_023435.1:g.44852C>T , LRG_162:g.44852C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314191.7:c.2420-1949C>T MANE Select	ENSP00000313420.3:n.2420-1949C>T
ENST00000314191.6:c.2420-1949C>T	ENSP00000313420.3:n.2420-1949C>T
ENST00000338368.7:c.2420-1949C>T	ENSP00000345182.4:n.2420-1949C>T
NM_001081640.1:c.2420-1949C>T	NP_001075109.1:n.2420-1949C>T
NM_006904.6:c.2420-1949C>T , LRG_162t1:c.2420-1949C>T	NP_008835.5:n.2420-1949C>T
XM_011517567.1:c.2420-1949C>T	XP_011515869.1:n.2420-1949C>T
XM_011517568.1:c.2420-1949C>T	XP_011515870.1:n.2420-1949C>T
NM_001081640.2:c.2420-1949C>T	NP_001075109.1:n.2420-1949C>T
NM_006904.7:c.2420-1949C>T MANE Select	NP_008835.5:n.2420-1949C>T