Canonical Allele Identifier: CA176169020

Gene: PRKDC

Linked Data

• dbSNP Id: rs1056494086
• gnomAD v3: 8-47852759-T-C
• gnomAD v4: 8-47852759-T-C
• MyVariant Identifiers: chr8:g.48765320T>C (hg19) ; chr8:g.47852759T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47852759T>C , CM000670.2:g.47852759T>C	GRCh38
NC_000008.10:g.48765320T>C , CM000670.1:g.48765320T>C	GRCh37
NC_000008.9:g.48927873T>C	NCBI36
NG_023435.1:g.112425A>G , LRG_162:g.112425A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000314191.7:c.6919A>G MANE Select	ENSP00000313420.3:p.Met2307Val
ENST00000314191.6:c.6919A>G	ENSP00000313420.3:p.Met2307Val
ENST00000338368.7:c.6919A>G	ENSP00000345182.4:p.Met2307Val
NM_001081640.1:c.6919A>G	NP_001075109.1:p.Met2307Val
NM_006904.6:c.6919A>G , LRG_162t1:c.6919A>G	NP_008835.5:p.Met2307Val
XM_011517567.1:c.6919A>G	XP_011515869.1:p.Met2307Val
XM_011517568.1:c.6919A>G	XP_011515870.1:p.Met2307Val
NM_001081640.2:c.6919A>G	NP_001075109.1:p.Met2307Val
NM_006904.7:c.6919A>G MANE Select	NP_008835.5:p.Met2307Val