Canonical Allele Identifier: CA2737775390

Linked Data

dbSNP Id: rs2146204969

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913155_18913156insG , CM000684.2:g.18913155_18913156insG GRCh38
NC_000022.10:g.18900668_18900669insG , CM000684.1:g.18900668_18900669insG GRCh37
NC_000022.9:g.17280668_17280669insG NCBI36
NG_008226.2:g.28398_28399insC
NG_009052.1:g.11933_11934insG
NG_008226.3:g.28398_28399insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*19_*20insC (PRODH) MANE Select ENSP00000349577.6:n.*19_*20insC
ENST00000638240.1:c.513+2127_513+2128insG ENSP00000492446.1:n.513+2127_513+2128insG
ENST00000313755.9:n.2587_2588insC (PRODH)
ENST00000334029.6:c.*19_*20insC (PRODH) ENSP00000334726.2:n.*19_*20insC
ENST00000357068.10:c.*19_*20insC (PRODH) ENSP00000349577.6:n.*19_*20insC
ENST00000420436.5:c.*19_*20insC (PRODH) ENSP00000410805.1:n.*19_*20insC
ENST00000429300.5:n.2193_2194insC (PRODH)
ENST00000482858.5:n.4302_4303insC (PRODH)
ENST00000483718.5:c.*1797_*1798insG (DGCR6) ENSP00000467483.1:n.*1797_*1798insG
ENST00000491604.5:n.2731_2732insC (PRODH)
ENST00000610940.4:c.*19_*20insC (PRODH) ENSP00000480347.1:n.*19_*20insC
NM_001195226.1:c.*19_*20insC (PRODH) NP_001182155.1:n.*19_*20insC
NM_016335.4:c.*19_*20insC (PRODH) NP_057419.4:n.*19_*20insC
XM_011530278.1:c.*19_*20insC (PRODH) XP_011528580.1:n.*19_*20insC
XM_011530279.1:c.*19_*20insC (PRODH) XP_011528581.1:n.*19_*20insC
XR_937876.1:n.1889_1890insC (PRODH)
NM_005675.5:c.*1466_*1467insG (DGCR6) NP_005666.2:n.*1466_*1467insG
NM_001195226.2:c.*19_*20insC (PRODH) NP_001182155.2:n.*19_*20insC
NM_016335.5:c.*19_*20insC (PRODH) NP_057419.5:n.*19_*20insC
NM_016335.6:c.*19_*20insC (PRODH) MANE Select NP_057419.5:n.*19_*20insC