Canonical Allele Identifier: CA2395633483

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913070G= , CM000684.2:g.18913070G= GRCh38
NC_000022.10:g.18900583G= , CM000684.1:g.18900583G= GRCh37
NC_000022.9:g.17280583G= NCBI36
NG_008226.2:g.28484C=
NG_009052.1:g.11848G=
NG_008226.3:g.28484C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*105C= (PRODH) MANE Select ENSP00000349577.6:n.*105C=
ENST00000638240.1:c.513+2042G= ENSP00000492446.1:n.513+2042G=
ENST00000313755.9:n.2673C= (PRODH)
ENST00000334029.6:c.*105C= (PRODH) ENSP00000334726.2:n.*105C=
ENST00000357068.10:c.*105C= (PRODH) ENSP00000349577.6:n.*105C=
ENST00000420436.5:c.*105C= (PRODH) ENSP00000410805.1:n.*105C=
ENST00000429300.5:n.2279C= (PRODH)
ENST00000482858.5:n.4388C= (PRODH)
ENST00000483718.5:c.*1712G= (DGCR6) ENSP00000467483.1:n.*1712G=
ENST00000491604.5:n.2817C= (PRODH)
ENST00000610940.4:c.*105C= (PRODH) ENSP00000480347.1:n.*105C=
NM_001195226.1:c.*105C= (PRODH) NP_001182155.1:n.*105C=
NM_016335.4:c.*105C= (PRODH) NP_057419.4:n.*105C=
XM_011530278.1:c.*105C= (PRODH) XP_011528580.1:n.*105C=
XM_011530279.1:c.*105C= (PRODH) XP_011528581.1:n.*105C=
XR_937876.1:n.1975C= (PRODH)
NM_005675.5:c.*1381G= (DGCR6) NP_005666.2:n.*1381G=
NM_001195226.2:c.*105C= (PRODH) NP_001182155.2:n.*105C=
NM_016335.5:c.*105C= (PRODH) NP_057419.5:n.*105C=
NM_016335.6:c.*105C= (PRODH) MANE Select NP_057419.5:n.*105C=