Canonical Allele Identifier: CA2395633539

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913167G= , CM000684.2:g.18913167G= GRCh38
NC_000022.10:g.18900680G= , CM000684.1:g.18900680G= GRCh37
NC_000022.9:g.17280680G= NCBI36
NG_008226.2:g.28387C=
NG_009052.1:g.11945G=
NG_008226.3:g.28387C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*8C= (PRODH) MANE Select ENSP00000349577.6:n.*8C=
ENST00000638240.1:c.513+2139G= ENSP00000492446.1:n.513+2139G=
ENST00000313755.9:n.2576C= (PRODH)
ENST00000334029.6:c.*8C= (PRODH) ENSP00000334726.2:n.*8C=
ENST00000357068.10:c.*8C= (PRODH) ENSP00000349577.6:n.*8C=
ENST00000420436.5:c.*8C= (PRODH) ENSP00000410805.1:n.*8C=
ENST00000429300.5:n.2182C= (PRODH)
ENST00000482858.5:n.4291C= (PRODH)
ENST00000483718.5:c.*1809G= (DGCR6) ENSP00000467483.1:n.*1809G=
ENST00000491604.5:n.2720C= (PRODH)
ENST00000610940.4:c.*8C= (PRODH) ENSP00000480347.1:n.*8C=
NM_001195226.1:c.*8C= (PRODH) NP_001182155.1:n.*8C=
NM_016335.4:c.*8C= (PRODH) NP_057419.4:n.*8C=
XM_011530278.1:c.*8C= (PRODH) XP_011528580.1:n.*8C=
XM_011530279.1:c.*8C= (PRODH) XP_011528581.1:n.*8C=
XR_937876.1:n.1878C= (PRODH)
NM_005675.5:c.*1478G= (DGCR6) NP_005666.2:n.*1478G=
NM_001195226.2:c.*8C= (PRODH) NP_001182155.2:n.*8C=
NM_016335.5:c.*8C= (PRODH) NP_057419.5:n.*8C=
NM_016335.6:c.*8C= (PRODH) MANE Select NP_057419.5:n.*8C=