Canonical Allele Identifier: CA2395633492

Linked Data

dbSNP Id: rs2081916737

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913083del , CM000684.2:g.18913083del GRCh38
NC_000022.10:g.18900596del , CM000684.1:g.18900596del GRCh37
NC_000022.9:g.17280596del NCBI36
NG_008226.2:g.28471del
NG_009052.1:g.11861del
NG_008226.3:g.28471del

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*92del (PRODH) MANE Select ENSP00000349577.6:n.*92del
ENST00000638240.1:c.513+2055del ENSP00000492446.1:n.513+2055del
ENST00000313755.9:n.2660del (PRODH)
ENST00000334029.6:c.*92del (PRODH) ENSP00000334726.2:n.*92del
ENST00000357068.10:c.*92del (PRODH) ENSP00000349577.6:n.*92del
ENST00000420436.5:c.*92del (PRODH) ENSP00000410805.1:n.*92del
ENST00000429300.5:n.2266del (PRODH)
ENST00000482858.5:n.4375del (PRODH)
ENST00000483718.5:c.*1725del (DGCR6) ENSP00000467483.1:n.*1725del
ENST00000491604.5:n.2804del (PRODH)
ENST00000610940.4:c.*92del (PRODH) ENSP00000480347.1:n.*92del
NM_001195226.1:c.*92del (PRODH) NP_001182155.1:n.*92del
NM_016335.4:c.*92del (PRODH) NP_057419.4:n.*92del
XM_011530278.1:c.*92del (PRODH) XP_011528580.1:n.*92del
XM_011530279.1:c.*92del (PRODH) XP_011528581.1:n.*92del
XR_937876.1:n.1962del (PRODH)
NM_005675.5:c.*1394del (DGCR6) NP_005666.2:n.*1394del
NM_001195226.2:c.*92del (PRODH) NP_001182155.2:n.*92del
NM_016335.5:c.*92del (PRODH) NP_057419.5:n.*92del
NM_016335.6:c.*92del (PRODH) MANE Select NP_057419.5:n.*92del