Canonical Allele Identifier: CA410637936

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913270T>G , CM000684.2:g.18913270T>G GRCh38
NC_000022.10:g.18900783T>G , CM000684.1:g.18900783T>G GRCh37
NC_000022.9:g.17280783T>G NCBI36
NG_008226.2:g.28284A>C
NG_009052.1:g.12048T>G
NG_008226.3:g.28284A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.1708A>C (PRODH) MANE Select ENSP00000349577.6:p.Ser570Arg
ENST00000638240.1:c.513+2242T>G ENSP00000492446.1:n.513+2242T>G
ENST00000313755.9:n.2473A>C (PRODH)
ENST00000334029.6:c.1384A>C (PRODH) ENSP00000334726.2:p.Ser462Arg
ENST00000357068.10:c.1708A>C (PRODH) ENSP00000349577.6:p.Ser570Arg
ENST00000420436.5:c.1384A>C (PRODH) ENSP00000410805.1:p.Ser462Arg
ENST00000429300.5:n.2079A>C (PRODH)
ENST00000482858.5:n.4188A>C (PRODH)
ENST00000483718.5:c.*1912T>G (DGCR6) ENSP00000467483.1:n.*1912T>G
ENST00000491604.5:n.2617A>C (PRODH)
ENST00000610940.4:c.1708A>C (PRODH) ENSP00000480347.1:p.Ser570Arg
NM_001195226.1:c.1384A>C (PRODH) NP_001182155.1:p.Ser462Arg
NM_016335.4:c.1708A>C (PRODH) NP_057419.4:p.Ser570Arg
XM_011530278.1:c.1135A>C (PRODH) XP_011528580.1:p.Ser379Arg
XM_011530279.1:c.928A>C (PRODH) XP_011528581.1:p.Ser310Arg
XR_937876.1:n.1775A>C (PRODH)
NM_005675.5:c.*1581T>G (DGCR6) NP_005666.2:n.*1581T>G
NM_001195226.2:c.1384A>C (PRODH) NP_001182155.2:p.Ser462Arg
NM_016335.5:c.1708A>C (PRODH) NP_057419.5:p.Ser570Arg
NM_016335.6:c.1708A>C (PRODH) MANE Select NP_057419.5:p.Ser570Arg