Canonical Allele Identifier: CA2395633497

Linked Data

dbSNP Id: rs2081916775

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913086del , CM000684.2:g.18913086del GRCh38
NC_000022.10:g.18900599del , CM000684.1:g.18900599del GRCh37
NC_000022.9:g.17280599del NCBI36
NG_008226.2:g.28469del
NG_009052.1:g.11864del
NG_008226.3:g.28469del

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*90del (PRODH) MANE Select ENSP00000349577.6:n.*90del
ENST00000638240.1:c.513+2058del ENSP00000492446.1:n.513+2058del
ENST00000313755.9:n.2658del (PRODH)
ENST00000334029.6:c.*90del (PRODH) ENSP00000334726.2:n.*90del
ENST00000357068.10:c.*90del (PRODH) ENSP00000349577.6:n.*90del
ENST00000420436.5:c.*90del (PRODH) ENSP00000410805.1:n.*90del
ENST00000429300.5:n.2264del (PRODH)
ENST00000482858.5:n.4373del (PRODH)
ENST00000483718.5:c.*1728del (DGCR6) ENSP00000467483.1:n.*1728del
ENST00000491604.5:n.2802del (PRODH)
ENST00000610940.4:c.*90del (PRODH) ENSP00000480347.1:n.*90del
NM_001195226.1:c.*90del (PRODH) NP_001182155.1:n.*90del
NM_016335.4:c.*90del (PRODH) NP_057419.4:n.*90del
XM_011530278.1:c.*90del (PRODH) XP_011528580.1:n.*90del
XM_011530279.1:c.*90del (PRODH) XP_011528581.1:n.*90del
XR_937876.1:n.1960del (PRODH)
NM_005675.5:c.*1397del (DGCR6) NP_005666.2:n.*1397del
NM_001195226.2:c.*90del (PRODH) NP_001182155.2:n.*90del
NM_016335.5:c.*90del (PRODH) NP_057419.5:n.*90del
NM_016335.6:c.*90del (PRODH) MANE Select NP_057419.5:n.*90del