Canonical Allele Identifier: CA460603575

Gene: PRKDC

Linked Data

• MyVariant Identifiers: chr8:g.48701497G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47788936G>T , CM000670.2:g.47788936G>T	GRCh38
NC_000008.10:g.48701497G>T , CM000670.1:g.48701497G>T	GRCh37
NC_000008.9:g.48864050G>T	NCBI36
NG_023435.1:g.176248C>A , LRG_162:g.176248C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697602.1:n.1445C>A
ENST00000697603.1:c.3549C>A	ENSP00000513358.1:p.Gly1183=
ENST00000314191.7:c.10872C>A MANE Select	ENSP00000313420.3:p.Gly3624=
ENST00000314191.6:c.10872C>A	ENSP00000313420.3:p.Gly3624=
ENST00000338368.7:c.10872C>A	ENSP00000345182.4:p.Gly3624=
NM_001081640.1:c.10872C>A	NP_001075109.1:p.Gly3624=
NM_006904.6:c.10872C>A , LRG_162t1:c.10872C>A	NP_008835.5:p.Gly3624=
XM_011517567.1:c.10875C>A	XP_011515869.1:p.Gly3625=
XM_011517568.1:c.10875C>A	XP_011515870.1:p.Gly3625=
NM_001081640.2:c.10872C>A	NP_001075109.1:p.Gly3624=
NM_006904.7:c.10872C>A MANE Select	NP_008835.5:p.Gly3624=