Canonical Allele Identifier: CA371137009

Gene: PRKDC

Linked Data

• gnomAD v4: 8-47817477-T-A
• MyVariant Identifiers: chr8:g.48730038T>A (hg19) ; chr8:g.47817477T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47817477T>A , CM000670.2:g.47817477T>A	GRCh38
NC_000008.10:g.48730038T>A , CM000670.1:g.48730038T>A	GRCh37
NC_000008.9:g.48892591T>A	NCBI36
NG_023435.1:g.147707A>T , LRG_162:g.147707A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697603.1:c.2207A>T	ENSP00000513358.1:p.Asn736Ile
ENST00000697607.1:n.1062A>T
ENST00000314191.7:c.9530A>T MANE Select	ENSP00000313420.3:p.Asn3177Ile
ENST00000314191.6:c.9530A>T	ENSP00000313420.3:p.Asn3177Ile
ENST00000338368.7:c.9530A>T	ENSP00000345182.4:p.Asn3177Ile
NM_001081640.1:c.9530A>T	NP_001075109.1:p.Asn3177Ile
NM_006904.6:c.9530A>T , LRG_162t1:c.9530A>T	NP_008835.5:p.Asn3177Ile
XM_011517567.1:c.9533A>T	XP_011515869.1:p.Asn3178Ile
XM_011517568.1:c.9533A>T	XP_011515870.1:p.Asn3178Ile
NM_001081640.2:c.9530A>T	NP_001075109.1:p.Asn3177Ile
NM_006904.7:c.9530A>T MANE Select	NP_008835.5:p.Asn3177Ile