Canonical Allele Identifier: CA1781897772
Gene: PRKDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47920324C= , CM000670.2:g.47920324C= GRCh38
NC_000008.10:g.48832884C= , CM000670.1:g.48832884C= GRCh37
NC_000008.9:g.48995437C= NCBI36
NG_023435.1:g.44860G= , LRG_162:g.44860G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314191.7:c.2420-1941G= MANE Select ENSP00000313420.3:n.2420-1941G=
ENST00000314191.6:c.2420-1941G= ENSP00000313420.3:n.2420-1941G=
ENST00000338368.7:c.2420-1941G= ENSP00000345182.4:n.2420-1941G=
NM_001081640.1:c.2420-1941G= NP_001075109.1:n.2420-1941G=
NM_006904.6:c.2420-1941G= , LRG_162t1:c.2420-1941G= NP_008835.5:n.2420-1941G=
XM_011517567.1:c.2420-1941G= XP_011515869.1:n.2420-1941G=
XM_011517568.1:c.2420-1941G= XP_011515870.1:n.2420-1941G=
NM_001081640.2:c.2420-1941G= NP_001075109.1:n.2420-1941G=
NM_006904.7:c.2420-1941G= MANE Select NP_008835.5:n.2420-1941G=