Canonical Allele Identifier: CA2395633565

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913224T= , CM000684.2:g.18913224T= GRCh38
NC_000022.10:g.18900737T= , CM000684.1:g.18900737T= GRCh37
NC_000022.9:g.17280737T= NCBI36
NG_008226.2:g.28330A=
NG_009052.1:g.12002T=
NG_008226.3:g.28330A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.1754A= (PRODH) MANE Select ENSP00000349577.6:p.Glu585=
ENST00000638240.1:c.513+2196T= ENSP00000492446.1:n.513+2196T=
ENST00000313755.9:n.2519A= (PRODH)
ENST00000334029.6:c.1430A= (PRODH) ENSP00000334726.2:p.Glu477=
ENST00000357068.10:c.1754A= (PRODH) ENSP00000349577.6:p.Glu585=
ENST00000420436.5:c.1430A= (PRODH) ENSP00000410805.1:p.Glu477=
ENST00000429300.5:n.2125A= (PRODH)
ENST00000482858.5:n.4234A= (PRODH)
ENST00000483718.5:c.*1866T= (DGCR6) ENSP00000467483.1:n.*1866T=
ENST00000491604.5:n.2663A= (PRODH)
ENST00000610940.4:c.1754A= (PRODH) ENSP00000480347.1:p.Glu585=
NM_001195226.1:c.1430A= (PRODH) NP_001182155.1:p.Glu477=
NM_016335.4:c.1754A= (PRODH) NP_057419.4:p.Glu585=
XM_011530278.1:c.1181A= (PRODH) XP_011528580.1:p.Glu394=
XM_011530279.1:c.974A= (PRODH) XP_011528581.1:p.Glu325=
XR_937876.1:n.1821A= (PRODH)
NM_005675.5:c.*1535T= (DGCR6) NP_005666.2:n.*1535T=
NM_001195226.2:c.1430A= (PRODH) NP_001182155.2:p.Glu477=
NM_016335.5:c.1754A= (PRODH) NP_057419.5:p.Glu585=
NM_016335.6:c.1754A= (PRODH) MANE Select NP_057419.5:p.Glu585=