Canonical Allele Identifier: CA2395633473

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913050C= , CM000684.2:g.18913050C= GRCh38
NC_000022.10:g.18900563C= , CM000684.1:g.18900563C= GRCh37
NC_000022.9:g.17280563C= NCBI36
NG_008226.2:g.28504G=
NG_009052.1:g.11828C=
NG_008226.3:g.28504G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*125G= (PRODH) MANE Select ENSP00000349577.6:n.*125G=
ENST00000638240.1:c.513+2022C= ENSP00000492446.1:n.513+2022C=
ENST00000313755.9:n.2693G= (PRODH)
ENST00000334029.6:c.*125G= (PRODH) ENSP00000334726.2:n.*125G=
ENST00000357068.10:c.*125G= (PRODH) ENSP00000349577.6:n.*125G=
ENST00000420436.5:c.*125G= (PRODH) ENSP00000410805.1:n.*125G=
ENST00000429300.5:n.2299G= (PRODH)
ENST00000482858.5:n.4408G= (PRODH)
ENST00000483718.5:c.*1692C= (DGCR6) ENSP00000467483.1:n.*1692C=
ENST00000491604.5:n.2837G= (PRODH)
ENST00000610940.4:c.*125G= (PRODH) ENSP00000480347.1:n.*125G=
NM_001195226.1:c.*125G= (PRODH) NP_001182155.1:n.*125G=
NM_016335.4:c.*125G= (PRODH) NP_057419.4:n.*125G=
XM_011530278.1:c.*125G= (PRODH) XP_011528580.1:n.*125G=
XM_011530279.1:c.*125G= (PRODH) XP_011528581.1:n.*125G=
XR_937876.1:n.1995G= (PRODH)
NM_005675.5:c.*1361C= (DGCR6) NP_005666.2:n.*1361C=
NM_001195226.2:c.*125G= (PRODH) NP_001182155.2:n.*125G=
NM_016335.5:c.*125G= (PRODH) NP_057419.5:n.*125G=
NM_016335.6:c.*125G= (PRODH) MANE Select NP_057419.5:n.*125G=