Canonical Allele Identifier: CA371132275

Gene: PRKDC

Linked Data

• dbSNP Id: rs1490966994
• gnomAD v2: 8-48701595-C-T
• gnomAD v4: 8-47789034-C-T
• MyVariant Identifiers: chr8:g.48701595C>T (hg19) ; chr8:g.47789034C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47789034C>T , CM000670.2:g.47789034C>T	GRCh38
NC_000008.10:g.48701595C>T , CM000670.1:g.48701595C>T	GRCh37
NC_000008.9:g.48864148C>T	NCBI36
NG_023435.1:g.176150G>A , LRG_162:g.176150G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697602.1:n.1347G>A
ENST00000697603.1:c.3451G>A	ENSP00000513358.1:p.Val1151Ile
ENST00000314191.7:c.10774G>A MANE Select	ENSP00000313420.3:p.Val3592Ile
ENST00000314191.6:c.10774G>A	ENSP00000313420.3:p.Val3592Ile
ENST00000338368.7:c.10774G>A	ENSP00000345182.4:p.Val3592Ile
NM_001081640.1:c.10774G>A	NP_001075109.1:p.Val3592Ile
NM_006904.6:c.10774G>A , LRG_162t1:c.10774G>A	NP_008835.5:p.Val3592Ile
XM_011517567.1:c.10777G>A	XP_011515869.1:p.Val3593Ile
XM_011517568.1:c.10777G>A	XP_011515870.1:p.Val3593Ile
NM_001081640.2:c.10774G>A	NP_001075109.1:p.Val3592Ile
NM_006904.7:c.10774G>A MANE Select	NP_008835.5:p.Val3592Ile