Canonical Allele Identifier: CA638502666

Linked Data

dbSNP Id: rs2081917051

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913137_18913138insGGGGGG , CM000684.2:g.18913137_18913138insGGGGGG GRCh38
NC_000022.10:g.18900650_18900651insGGGGGG , CM000684.1:g.18900650_18900651insGGGGGG GRCh37
NC_000022.9:g.17280650_17280651insGGGGGG NCBI36
NG_008226.2:g.28421_28422insCCCCCC
NG_009052.1:g.11915_11916insGGGGGG
NG_008226.3:g.28421_28422insCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*42_*43insCCCCCC (PRODH) MANE Select ENSP00000349577.6:n.*42_*43insCCCCCC
ENST00000638240.1:c.513+2109_513+2110insGGGGGG ENSP00000492446.1:n.513+2109_513+2110insGGGGGG
ENST00000313755.9:n.2610_2611insCCCCCC (PRODH)
ENST00000334029.6:c.*42_*43insCCCCCC (PRODH) ENSP00000334726.2:n.*42_*43insCCCCCC
ENST00000357068.10:c.*42_*43insCCCCCC (PRODH) ENSP00000349577.6:n.*42_*43insCCCCCC
ENST00000420436.5:c.*42_*43insCCCCCC (PRODH) ENSP00000410805.1:n.*42_*43insCCCCCC
ENST00000429300.5:n.2216_2217insCCCCCC (PRODH)
ENST00000482858.5:n.4325_4326insCCCCCC (PRODH)
ENST00000483718.5:c.*1779_*1780insGGGGGG (DGCR6) ENSP00000467483.1:n.*1779_*1780insGGGGGG
ENST00000491604.5:n.2754_2755insCCCCCC (PRODH)
ENST00000610940.4:c.*42_*43insCCCCCC (PRODH) ENSP00000480347.1:n.*42_*43insCCCCCC
NM_001195226.1:c.*42_*43insCCCCCC (PRODH) NP_001182155.1:n.*42_*43insCCCCCC
NM_016335.4:c.*42_*43insCCCCCC (PRODH) NP_057419.4:n.*42_*43insCCCCCC
XM_011530278.1:c.*42_*43insCCCCCC (PRODH) XP_011528580.1:n.*42_*43insCCCCCC
XM_011530279.1:c.*42_*43insCCCCCC (PRODH) XP_011528581.1:n.*42_*43insCCCCCC
XR_937876.1:n.1912_1913insCCCCCC (PRODH)
NM_005675.5:c.*1448_*1449insGGGGGG (DGCR6) NP_005666.2:n.*1448_*1449insGGGGGG
NM_001195226.2:c.*42_*43insCCCCCC (PRODH) NP_001182155.2:n.*42_*43insCCCCCC
NM_016335.5:c.*42_*43insCCCCCC (PRODH) NP_057419.5:n.*42_*43insCCCCCC
NM_016335.6:c.*42_*43insCCCCCC (PRODH) MANE Select NP_057419.5:n.*42_*43insCCCCCC