Canonical Allele Identifier: CA2395633711

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913545G= , CM000684.2:g.18913545G= GRCh38
NC_000022.10:g.18901058G= , CM000684.1:g.18901058G= GRCh37
NC_000022.9:g.17281058G= NCBI36
NG_008226.2:g.28009C=
NG_009052.1:g.12323G=
NG_008226.3:g.28009C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.1527-19C= (PRODH) MANE Select ENSP00000349577.6:n.1527-19C=
ENST00000638240.1:c.513+2517G= ENSP00000492446.1:n.513+2517G=
ENST00000313755.9:n.2292-19C= (PRODH)
ENST00000334029.6:c.1203-19C= (PRODH) ENSP00000334726.2:n.1203-19C=
ENST00000357068.10:c.1527-19C= (PRODH) ENSP00000349577.6:n.1527-19C=
ENST00000420436.5:c.1203-19C= (PRODH) ENSP00000410805.1:n.1203-19C=
ENST00000429300.5:n.1898-19C= (PRODH)
ENST00000482858.5:n.4007-19C= (PRODH)
ENST00000483718.5:c.*2187G= (DGCR6) ENSP00000467483.1:n.*2187G=
ENST00000491604.5:n.2436-19C= (PRODH)
ENST00000610940.4:c.1527-19C= (PRODH) ENSP00000480347.1:n.1527-19C=
NM_001195226.1:c.1203-19C= (PRODH) NP_001182155.1:n.1203-19C=
NM_016335.4:c.1527-19C= (PRODH) NP_057419.4:n.1527-19C=
XM_011530278.1:c.954-19C= (PRODH) XP_011528580.1:n.954-19C=
XM_011530279.1:c.747-19C= (PRODH) XP_011528581.1:n.747-19C=
XR_937876.1:n.1594-19C= (PRODH)
NM_005675.5:c.*1856G= (DGCR6) NP_005666.2:n.*1856G=
NM_001195226.2:c.1203-19C= (PRODH) NP_001182155.2:n.1203-19C=
NM_016335.5:c.1527-19C= (PRODH) NP_057419.5:n.1527-19C=
NM_016335.6:c.1527-19C= (PRODH) MANE Select NP_057419.5:n.1527-19C=