Canonical Allele Identifier: CA2395633517

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913138_18913139delinsCG , CM000684.2:g.18913138_18913139delinsCG GRCh38
NC_000022.10:g.18900651_18900652delinsCG , CM000684.1:g.18900651_18900652delinsCG GRCh37
NC_000022.9:g.17280651_17280652delinsCG NCBI36
NG_008226.2:g.28415_28416delinsCG
NG_009052.1:g.11916_11917delinsCG
NG_008226.3:g.28415_28416delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*36_*37delinsCG (PRODH) MANE Select ENSP00000349577.6:n.*36_*37delinsCG
ENST00000638240.1:c.513+2110_513+2111delinsCG ENSP00000492446.1:n.513+2110_513+2111delinsCG
ENST00000313755.9:n.2604_2605delinsCG (PRODH)
ENST00000334029.6:c.*36_*37delinsCG (PRODH) ENSP00000334726.2:n.*36_*37delinsCG
ENST00000357068.10:c.*36_*37delinsCG (PRODH) ENSP00000349577.6:n.*36_*37delinsCG
ENST00000420436.5:c.*36_*37delinsCG (PRODH) ENSP00000410805.1:n.*36_*37delinsCG
ENST00000429300.5:n.2210_2211delinsCG (PRODH)
ENST00000482858.5:n.4319_4320delinsCG (PRODH)
ENST00000483718.5:c.*1780_*1781delinsCG (DGCR6) ENSP00000467483.1:n.*1780_*1781delinsCG
ENST00000491604.5:n.2748_2749delinsCG (PRODH)
ENST00000610940.4:c.*36_*37delinsCG (PRODH) ENSP00000480347.1:n.*36_*37delinsCG
NM_001195226.1:c.*36_*37delinsCG (PRODH) NP_001182155.1:n.*36_*37delinsCG
NM_016335.4:c.*36_*37delinsCG (PRODH) NP_057419.4:n.*36_*37delinsCG
XM_011530278.1:c.*36_*37delinsCG (PRODH) XP_011528580.1:n.*36_*37delinsCG
XM_011530279.1:c.*36_*37delinsCG (PRODH) XP_011528581.1:n.*36_*37delinsCG
XR_937876.1:n.1906_1907delinsCG (PRODH)
NM_005675.5:c.*1449_*1450delinsCG (DGCR6) NP_005666.2:n.*1449_*1450delinsCG
NM_001195226.2:c.*36_*37delinsCG (PRODH) NP_001182155.2:n.*36_*37delinsCG
NM_016335.5:c.*36_*37delinsCG (PRODH) NP_057419.5:n.*36_*37delinsCG
NM_016335.6:c.*36_*37delinsCG (PRODH) MANE Select NP_057419.5:n.*36_*37delinsCG