Canonical Allele Identifier: CA2395633516

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913138C= , CM000684.2:g.18913138C= GRCh38
NC_000022.10:g.18900651C= , CM000684.1:g.18900651C= GRCh37
NC_000022.9:g.17280651C= NCBI36
NG_008226.2:g.28416G=
NG_009052.1:g.11916C=
NG_008226.3:g.28416G=

Transcript Alleles

HGVS Amino-acid change
ENST00000357068.11:c.*37G= (PRODH) MANE Select ENSP00000349577.6:n.*37G=
ENST00000638240.1:c.513+2110C= ENSP00000492446.1:n.513+2110C=
ENST00000313755.9:n.2605G= (PRODH)
ENST00000334029.6:c.*37G= (PRODH) ENSP00000334726.2:n.*37G=
ENST00000357068.10:c.*37G= (PRODH) ENSP00000349577.6:n.*37G=
ENST00000420436.5:c.*37G= (PRODH) ENSP00000410805.1:n.*37G=
ENST00000429300.5:n.2211G= (PRODH)
ENST00000482858.5:n.4320G= (PRODH)
ENST00000483718.5:c.*1780C= (DGCR6) ENSP00000467483.1:n.*1780C=
ENST00000491604.5:n.2749G= (PRODH)
ENST00000610940.4:c.*37G= (PRODH) ENSP00000480347.1:n.*37G=
NM_001195226.1:c.*37G= (PRODH) NP_001182155.1:n.*37G=
NM_016335.4:c.*37G= (PRODH) NP_057419.4:n.*37G=
XM_011530278.1:c.*37G= (PRODH) XP_011528580.1:n.*37G=
XM_011530279.1:c.*37G= (PRODH) XP_011528581.1:n.*37G=
XR_937876.1:n.1907G= (PRODH)
NM_005675.5:c.*1449C= (DGCR6) NP_005666.2:n.*1449C=
NM_001195226.2:c.*37G= (PRODH) NP_001182155.2:n.*37G=
NM_016335.5:c.*37G= (PRODH) NP_057419.5:n.*37G=
NM_016335.6:c.*37G= (PRODH) MANE Select NP_057419.5:n.*37G=