Canonical Allele Identifier: CA2395633491

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913082_18913083delinsGT , CM000684.2:g.18913082_18913083delinsGT GRCh38
NC_000022.10:g.18900595_18900596delinsGT , CM000684.1:g.18900595_18900596delinsGT GRCh37
NC_000022.9:g.17280595_17280596delinsGT NCBI36
NG_008226.2:g.28471_28472delinsAC
NG_009052.1:g.11860_11861delinsGT
NG_008226.3:g.28471_28472delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*92_*93delinsAC (PRODH) MANE Select ENSP00000349577.6:n.*92_*93delinsAC
ENST00000638240.1:c.513+2054_513+2055delinsGT ENSP00000492446.1:n.513+2054_513+2055delinsGT
ENST00000313755.9:n.2660_2661delinsAC (PRODH)
ENST00000334029.6:c.*92_*93delinsAC (PRODH) ENSP00000334726.2:n.*92_*93delinsAC
ENST00000357068.10:c.*92_*93delinsAC (PRODH) ENSP00000349577.6:n.*92_*93delinsAC
ENST00000420436.5:c.*92_*93delinsAC (PRODH) ENSP00000410805.1:n.*92_*93delinsAC
ENST00000429300.5:n.2266_2267delinsAC (PRODH)
ENST00000482858.5:n.4375_4376delinsAC (PRODH)
ENST00000483718.5:c.*1724_*1725delinsGT (DGCR6) ENSP00000467483.1:n.*1724_*1725delinsGT
ENST00000491604.5:n.2804_2805delinsAC (PRODH)
ENST00000610940.4:c.*92_*93delinsAC (PRODH) ENSP00000480347.1:n.*92_*93delinsAC
NM_001195226.1:c.*92_*93delinsAC (PRODH) NP_001182155.1:n.*92_*93delinsAC
NM_016335.4:c.*92_*93delinsAC (PRODH) NP_057419.4:n.*92_*93delinsAC
XM_011530278.1:c.*92_*93delinsAC (PRODH) XP_011528580.1:n.*92_*93delinsAC
XM_011530279.1:c.*92_*93delinsAC (PRODH) XP_011528581.1:n.*92_*93delinsAC
XR_937876.1:n.1962_1963delinsAC (PRODH)
NM_005675.5:c.*1393_*1394delinsGT (DGCR6) NP_005666.2:n.*1393_*1394delinsGT
NM_001195226.2:c.*92_*93delinsAC (PRODH) NP_001182155.2:n.*92_*93delinsAC
NM_016335.5:c.*92_*93delinsAC (PRODH) NP_057419.5:n.*92_*93delinsAC
NM_016335.6:c.*92_*93delinsAC (PRODH) MANE Select NP_057419.5:n.*92_*93delinsAC