Canonical Allele Identifier: CA2818372182

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913131_18913132insGGGG , CM000684.2:g.18913131_18913132insGGGG GRCh38
NC_000022.10:g.18900644_18900645insGGGG , CM000684.1:g.18900644_18900645insGGGG GRCh37
NC_000022.9:g.17280644_17280645insGGGG NCBI36
NG_008226.2:g.28425_28426insCCCC
NG_009052.1:g.11909_11910insGGGG
NG_008226.3:g.28425_28426insCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*46_*47insCCCC (PRODH) MANE Select ENSP00000349577.6:n.*46_*47insCCCC
ENST00000638240.1:c.513+2103_513+2104insGGGG ENSP00000492446.1:n.513+2103_513+2104insGGGG
ENST00000313755.9:n.2614_2615insCCCC (PRODH)
ENST00000334029.6:c.*46_*47insCCCC (PRODH) ENSP00000334726.2:n.*46_*47insCCCC
ENST00000357068.10:c.*46_*47insCCCC (PRODH) ENSP00000349577.6:n.*46_*47insCCCC
ENST00000420436.5:c.*46_*47insCCCC (PRODH) ENSP00000410805.1:n.*46_*47insCCCC
ENST00000429300.5:n.2220_2221insCCCC (PRODH)
ENST00000482858.5:n.4329_4330insCCCC (PRODH)
ENST00000483718.5:c.*1773_*1774insGGGG (DGCR6) ENSP00000467483.1:n.*1773_*1774insGGGG
ENST00000491604.5:n.2758_2759insCCCC (PRODH)
ENST00000610940.4:c.*46_*47insCCCC (PRODH) ENSP00000480347.1:n.*46_*47insCCCC
NM_001195226.1:c.*46_*47insCCCC (PRODH) NP_001182155.1:n.*46_*47insCCCC
NM_016335.4:c.*46_*47insCCCC (PRODH) NP_057419.4:n.*46_*47insCCCC
XM_011530278.1:c.*46_*47insCCCC (PRODH) XP_011528580.1:n.*46_*47insCCCC
XM_011530279.1:c.*46_*47insCCCC (PRODH) XP_011528581.1:n.*46_*47insCCCC
XR_937876.1:n.1916_1917insCCCC (PRODH)
NM_005675.5:c.*1442_*1443insGGGG (DGCR6) NP_005666.2:n.*1442_*1443insGGGG
NM_001195226.2:c.*46_*47insCCCC (PRODH) NP_001182155.2:n.*46_*47insCCCC
NM_016335.5:c.*46_*47insCCCC (PRODH) NP_057419.5:n.*46_*47insCCCC
NM_016335.6:c.*46_*47insCCCC (PRODH) MANE Select NP_057419.5:n.*46_*47insCCCC