Canonical Allele Identifier: CA410637880

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913261T>G , CM000684.2:g.18913261T>G GRCh38
NC_000022.10:g.18900774T>G , CM000684.1:g.18900774T>G GRCh37
NC_000022.9:g.17280774T>G NCBI36
NG_008226.2:g.28293A>C
NG_009052.1:g.12039T>G
NG_008226.3:g.28293A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.1717A>C (PRODH) MANE Select ENSP00000349577.6:p.Lys573Gln
ENST00000638240.1:c.513+2233T>G ENSP00000492446.1:n.513+2233T>G
ENST00000313755.9:n.2482A>C (PRODH)
ENST00000334029.6:c.1393A>C (PRODH) ENSP00000334726.2:p.Lys465Gln
ENST00000357068.10:c.1717A>C (PRODH) ENSP00000349577.6:p.Lys573Gln
ENST00000420436.5:c.1393A>C (PRODH) ENSP00000410805.1:p.Lys465Gln
ENST00000429300.5:n.2088A>C (PRODH)
ENST00000482858.5:n.4197A>C (PRODH)
ENST00000483718.5:c.*1903T>G (DGCR6) ENSP00000467483.1:n.*1903T>G
ENST00000491604.5:n.2626A>C (PRODH)
ENST00000610940.4:c.1717A>C (PRODH) ENSP00000480347.1:p.Lys573Gln
NM_001195226.1:c.1393A>C (PRODH) NP_001182155.1:p.Lys465Gln
NM_016335.4:c.1717A>C (PRODH) NP_057419.4:p.Lys573Gln
XM_011530278.1:c.1144A>C (PRODH) XP_011528580.1:p.Lys382Gln
XM_011530279.1:c.937A>C (PRODH) XP_011528581.1:p.Lys313Gln
XR_937876.1:n.1784A>C (PRODH)
NM_005675.5:c.*1572T>G (DGCR6) NP_005666.2:n.*1572T>G
NM_001195226.2:c.1393A>C (PRODH) NP_001182155.2:p.Lys465Gln
NM_016335.5:c.1717A>C (PRODH) NP_057419.5:p.Lys573Gln
NM_016335.6:c.1717A>C (PRODH) MANE Select NP_057419.5:p.Lys573Gln