Canonical Allele Identifier: CA410638040

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913290C>A , CM000684.2:g.18913290C>A GRCh38
NC_000022.10:g.18900803C>A , CM000684.1:g.18900803C>A GRCh37
NC_000022.9:g.17280803C>A NCBI36
NG_008226.2:g.28264G>T
NG_009052.1:g.12068C>A
NG_008226.3:g.28264G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.1688G>T (PRODH) MANE Select ENSP00000349577.6:p.Arg563Leu
ENST00000638240.1:c.513+2262C>A ENSP00000492446.1:n.513+2262C>A
ENST00000313755.9:n.2453G>T (PRODH)
ENST00000334029.6:c.1364G>T (PRODH) ENSP00000334726.2:p.Arg455Leu
ENST00000357068.10:c.1688G>T (PRODH) ENSP00000349577.6:p.Arg563Leu
ENST00000420436.5:c.1364G>T (PRODH) ENSP00000410805.1:p.Arg455Leu
ENST00000429300.5:n.2059G>T (PRODH)
ENST00000482858.5:n.4168G>T (PRODH)
ENST00000483718.5:c.*1932C>A (DGCR6) ENSP00000467483.1:n.*1932C>A
ENST00000491604.5:n.2597G>T (PRODH)
ENST00000610940.4:c.1688G>T (PRODH) ENSP00000480347.1:p.Arg563Leu
NM_001195226.1:c.1364G>T (PRODH) NP_001182155.1:p.Arg455Leu
NM_016335.4:c.1688G>T (PRODH) NP_057419.4:p.Arg563Leu
XM_011530278.1:c.1115G>T (PRODH) XP_011528580.1:p.Arg372Leu
XM_011530279.1:c.908G>T (PRODH) XP_011528581.1:p.Arg303Leu
XR_937876.1:n.1755G>T (PRODH)
NM_005675.5:c.*1601C>A (DGCR6) NP_005666.2:n.*1601C>A
NM_001195226.2:c.1364G>T (PRODH) NP_001182155.2:p.Arg455Leu
NM_016335.5:c.1688G>T (PRODH) NP_057419.5:p.Arg563Leu
NM_016335.6:c.1688G>T (PRODH) MANE Select NP_057419.5:p.Arg563Leu