Canonical Allele Identifier: CA10094869

Linked Data

dbSNP Id: rs762463680

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913395dup , CM000684.2:g.18913395dup GRCh38
NC_000022.10:g.18900908dup , CM000684.1:g.18900908dup GRCh37
NC_000022.9:g.17280908dup NCBI36
NG_008226.2:g.28160dup
NG_009052.1:g.12173dup
NG_008226.3:g.28160dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.1616-32dup (PRODH) MANE Select ENSP00000349577.6:n.1616-32dup
ENST00000638240.1:c.513+2367dup ENSP00000492446.1:n.513+2367dup
ENST00000313755.9:n.2381-32dup (PRODH)
ENST00000334029.6:c.1292-32dup (PRODH) ENSP00000334726.2:n.1292-32dup
ENST00000357068.10:c.1616-32dup (PRODH) ENSP00000349577.6:n.1616-32dup
ENST00000420436.5:c.1292-32dup (PRODH) ENSP00000410805.1:n.1292-32dup
ENST00000429300.5:n.1987-32dup (PRODH)
ENST00000482858.5:n.4096-32dup (PRODH)
ENST00000483718.5:c.*2037dup (DGCR6) ENSP00000467483.1:n.*2037dup
ENST00000491604.5:n.2525-32dup (PRODH)
ENST00000610940.4:c.1616-32dup (PRODH) ENSP00000480347.1:n.1616-32dup
NM_001195226.1:c.1292-32dup (PRODH) NP_001182155.1:n.1292-32dup
NM_016335.4:c.1616-32dup (PRODH) NP_057419.4:n.1616-32dup
XM_011530278.1:c.1043-32dup (PRODH) XP_011528580.1:n.1043-32dup
XM_011530279.1:c.836-32dup (PRODH) XP_011528581.1:n.836-32dup
XR_937876.1:n.1683-32dup (PRODH)
NM_005675.5:c.*1706dup (DGCR6) NP_005666.2:n.*1706dup
NM_001195226.2:c.1292-32dup (PRODH) NP_001182155.2:n.1292-32dup
NM_016335.5:c.1616-32dup (PRODH) NP_057419.5:n.1616-32dup
NM_016335.6:c.1616-32dup (PRODH) MANE Select NP_057419.5:n.1616-32dup