Canonical Allele Identifier: CA2395633481

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913068T= , CM000684.2:g.18913068T= GRCh38
NC_000022.10:g.18900581T= , CM000684.1:g.18900581T= GRCh37
NC_000022.9:g.17280581T= NCBI36
NG_008226.2:g.28486A=
NG_009052.1:g.11846T=
NG_008226.3:g.28486A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*107A= (PRODH) MANE Select ENSP00000349577.6:n.*107A=
ENST00000638240.1:c.513+2040T= ENSP00000492446.1:n.513+2040T=
ENST00000313755.9:n.2675A= (PRODH)
ENST00000334029.6:c.*107A= (PRODH) ENSP00000334726.2:n.*107A=
ENST00000357068.10:c.*107A= (PRODH) ENSP00000349577.6:n.*107A=
ENST00000420436.5:c.*107A= (PRODH) ENSP00000410805.1:n.*107A=
ENST00000429300.5:n.2281A= (PRODH)
ENST00000482858.5:n.4390A= (PRODH)
ENST00000483718.5:c.*1710T= (DGCR6) ENSP00000467483.1:n.*1710T=
ENST00000491604.5:n.2819A= (PRODH)
ENST00000610940.4:c.*107A= (PRODH) ENSP00000480347.1:n.*107A=
NM_001195226.1:c.*107A= (PRODH) NP_001182155.1:n.*107A=
NM_016335.4:c.*107A= (PRODH) NP_057419.4:n.*107A=
XM_011530278.1:c.*107A= (PRODH) XP_011528580.1:n.*107A=
XM_011530279.1:c.*107A= (PRODH) XP_011528581.1:n.*107A=
XR_937876.1:n.1977A= (PRODH)
NM_005675.5:c.*1379T= (DGCR6) NP_005666.2:n.*1379T=
NM_001195226.2:c.*107A= (PRODH) NP_001182155.2:n.*107A=
NM_016335.5:c.*107A= (PRODH) NP_057419.5:n.*107A=
NM_016335.6:c.*107A= (PRODH) MANE Select NP_057419.5:n.*107A=