Canonical Allele Identifier: CA2395633485

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913074_18913076delinsGAA , CM000684.2:g.18913074_18913076delinsGAA GRCh38
NC_000022.10:g.18900587_18900589delinsGAA , CM000684.1:g.18900587_18900589delinsGAA GRCh37
NC_000022.9:g.17280587_17280589delinsGAA NCBI36
NG_008226.2:g.28478_28480delinsTTC
NG_009052.1:g.11852_11854delinsGAA
NG_008226.3:g.28478_28480delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*99_*101delinsTTC (PRODH) MANE Select ENSP00000349577.6:n.*99_*101delinsTTC
ENST00000638240.1:c.513+2046_513+2048delinsGAA ENSP00000492446.1:n.513+2046_513+2048delinsGAA
ENST00000313755.9:n.2667_2669delinsTTC (PRODH)
ENST00000334029.6:c.*99_*101delinsTTC (PRODH) ENSP00000334726.2:n.*99_*101delinsTTC
ENST00000357068.10:c.*99_*101delinsTTC (PRODH) ENSP00000349577.6:n.*99_*101delinsTTC
ENST00000420436.5:c.*99_*101delinsTTC (PRODH) ENSP00000410805.1:n.*99_*101delinsTTC
ENST00000429300.5:n.2273_2275delinsTTC (PRODH)
ENST00000482858.5:n.4382_4384delinsTTC (PRODH)
ENST00000483718.5:c.*1716_*1718delinsGAA (DGCR6) ENSP00000467483.1:n.*1716_*1718delinsGAA
ENST00000491604.5:n.2811_2813delinsTTC (PRODH)
ENST00000610940.4:c.*99_*101delinsTTC (PRODH) ENSP00000480347.1:n.*99_*101delinsTTC
NM_001195226.1:c.*99_*101delinsTTC (PRODH) NP_001182155.1:n.*99_*101delinsTTC
NM_016335.4:c.*99_*101delinsTTC (PRODH) NP_057419.4:n.*99_*101delinsTTC
XM_011530278.1:c.*99_*101delinsTTC (PRODH) XP_011528580.1:n.*99_*101delinsTTC
XM_011530279.1:c.*99_*101delinsTTC (PRODH) XP_011528581.1:n.*99_*101delinsTTC
XR_937876.1:n.1969_1971delinsTTC (PRODH)
NM_005675.5:c.*1385_*1387delinsGAA (DGCR6) NP_005666.2:n.*1385_*1387delinsGAA
NM_001195226.2:c.*99_*101delinsTTC (PRODH) NP_001182155.2:n.*99_*101delinsTTC
NM_016335.5:c.*99_*101delinsTTC (PRODH) NP_057419.5:n.*99_*101delinsTTC
NM_016335.6:c.*99_*101delinsTTC (PRODH) MANE Select NP_057419.5:n.*99_*101delinsTTC