Canonical Allele Identifier: CA2395633535

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913159G= , CM000684.2:g.18913159G= GRCh38
NC_000022.10:g.18900672G= , CM000684.1:g.18900672G= GRCh37
NC_000022.9:g.17280672G= NCBI36
NG_008226.2:g.28395C=
NG_009052.1:g.11937G=
NG_008226.3:g.28395C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*16C= (PRODH) MANE Select ENSP00000349577.6:n.*16C=
ENST00000638240.1:c.513+2131G= ENSP00000492446.1:n.513+2131G=
ENST00000313755.9:n.2584C= (PRODH)
ENST00000334029.6:c.*16C= (PRODH) ENSP00000334726.2:n.*16C=
ENST00000357068.10:c.*16C= (PRODH) ENSP00000349577.6:n.*16C=
ENST00000420436.5:c.*16C= (PRODH) ENSP00000410805.1:n.*16C=
ENST00000429300.5:n.2190C= (PRODH)
ENST00000482858.5:n.4299C= (PRODH)
ENST00000483718.5:c.*1801G= (DGCR6) ENSP00000467483.1:n.*1801G=
ENST00000491604.5:n.2728C= (PRODH)
ENST00000610940.4:c.*16C= (PRODH) ENSP00000480347.1:n.*16C=
NM_001195226.1:c.*16C= (PRODH) NP_001182155.1:n.*16C=
NM_016335.4:c.*16C= (PRODH) NP_057419.4:n.*16C=
XM_011530278.1:c.*16C= (PRODH) XP_011528580.1:n.*16C=
XM_011530279.1:c.*16C= (PRODH) XP_011528581.1:n.*16C=
XR_937876.1:n.1886C= (PRODH)
NM_005675.5:c.*1470G= (DGCR6) NP_005666.2:n.*1470G=
NM_001195226.2:c.*16C= (PRODH) NP_001182155.2:n.*16C=
NM_016335.5:c.*16C= (PRODH) NP_057419.5:n.*16C=
NM_016335.6:c.*16C= (PRODH) MANE Select NP_057419.5:n.*16C=