Canonical Allele Identifier: CA10094898

Linked Data

dbSNP Id: rs756739806

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913554dup , CM000684.2:g.18913554dup GRCh38
NC_000022.10:g.18901067dup , CM000684.1:g.18901067dup GRCh37
NC_000022.9:g.17281067dup NCBI36
NG_008226.2:g.28002dup
NG_009052.1:g.12332dup
NG_008226.3:g.28002dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.1527-26dup (PRODH) MANE Select ENSP00000349577.6:n.1527-26dup
ENST00000638240.1:c.513+2526dup ENSP00000492446.1:n.513+2526dup
ENST00000313755.9:n.2292-26dup (PRODH)
ENST00000334029.6:c.1203-26dup (PRODH) ENSP00000334726.2:n.1203-26dup
ENST00000357068.10:c.1527-26dup (PRODH) ENSP00000349577.6:n.1527-26dup
ENST00000420436.5:c.1203-26dup (PRODH) ENSP00000410805.1:n.1203-26dup
ENST00000429300.5:n.1898-26dup (PRODH)
ENST00000482858.5:n.4007-26dup (PRODH)
ENST00000483718.5:c.*2196dup (DGCR6) ENSP00000467483.1:n.*2196dup
ENST00000491604.5:n.2436-26dup (PRODH)
ENST00000610940.4:c.1527-26dup (PRODH) ENSP00000480347.1:n.1527-26dup
NM_001195226.1:c.1203-26dup (PRODH) NP_001182155.1:n.1203-26dup
NM_016335.4:c.1527-26dup (PRODH) NP_057419.4:n.1527-26dup
XM_011530278.1:c.954-26dup (PRODH) XP_011528580.1:n.954-26dup
XM_011530279.1:c.747-26dup (PRODH) XP_011528581.1:n.747-26dup
XR_937876.1:n.1594-26dup (PRODH)
NM_005675.5:c.*1865dup (DGCR6) NP_005666.2:n.*1865dup
NM_001195226.2:c.1203-26dup (PRODH) NP_001182155.2:n.1203-26dup
NM_016335.5:c.1527-26dup (PRODH) NP_057419.5:n.1527-26dup
NM_016335.6:c.1527-26dup (PRODH) MANE Select NP_057419.5:n.1527-26dup