Canonical Allele Identifier: CA2655228904

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913160del , CM000684.2:g.18913160del GRCh38
NC_000022.10:g.18900673del , CM000684.1:g.18900673del GRCh37
NC_000022.9:g.17280673del NCBI36
NG_008226.2:g.28396del
NG_009052.1:g.11938del
NG_008226.3:g.28396del

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*17del (PRODH) MANE Select ENSP00000349577.6:n.*17del
ENST00000638240.1:c.513+2132del ENSP00000492446.1:n.513+2132del
ENST00000313755.9:n.2585del (PRODH)
ENST00000334029.6:c.*17del (PRODH) ENSP00000334726.2:n.*17del
ENST00000357068.10:c.*17del (PRODH) ENSP00000349577.6:n.*17del
ENST00000420436.5:c.*17del (PRODH) ENSP00000410805.1:n.*17del
ENST00000429300.5:n.2191del (PRODH)
ENST00000482858.5:n.4300del (PRODH)
ENST00000483718.5:c.*1802del (DGCR6) ENSP00000467483.1:n.*1802del
ENST00000491604.5:n.2729del (PRODH)
ENST00000610940.4:c.*17del (PRODH) ENSP00000480347.1:n.*17del
NM_001195226.1:c.*17del (PRODH) NP_001182155.1:n.*17del
NM_016335.4:c.*17del (PRODH) NP_057419.4:n.*17del
XM_011530278.1:c.*17del (PRODH) XP_011528580.1:n.*17del
XM_011530279.1:c.*17del (PRODH) XP_011528581.1:n.*17del
XR_937876.1:n.1887del (PRODH)
NM_005675.5:c.*1471del (DGCR6) NP_005666.2:n.*1471del
NM_001195226.2:c.*17del (PRODH) NP_001182155.2:n.*17del
NM_016335.5:c.*17del (PRODH) NP_057419.5:n.*17del
NM_016335.6:c.*17del (PRODH) MANE Select NP_057419.5:n.*17del