Canonical Allele Identifier: CA1024068791

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913087T>G , CM000684.2:g.18913087T>G GRCh38
NC_000022.10:g.18900600T>G , CM000684.1:g.18900600T>G GRCh37
NC_000022.9:g.17280600T>G NCBI36
NG_008226.2:g.28467A>C
NG_009052.1:g.11865T>G
NG_008226.3:g.28467A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*88A>C (PRODH) MANE Select ENSP00000349577.6:n.*88A>C
ENST00000638240.1:c.513+2059T>G ENSP00000492446.1:n.513+2059T>G
ENST00000313755.9:n.2656A>C (PRODH)
ENST00000334029.6:c.*88A>C (PRODH) ENSP00000334726.2:n.*88A>C
ENST00000357068.10:c.*88A>C (PRODH) ENSP00000349577.6:n.*88A>C
ENST00000420436.5:c.*88A>C (PRODH) ENSP00000410805.1:n.*88A>C
ENST00000429300.5:n.2262A>C (PRODH)
ENST00000482858.5:n.4371A>C (PRODH)
ENST00000483718.5:c.*1729T>G (DGCR6) ENSP00000467483.1:n.*1729T>G
ENST00000491604.5:n.2800A>C (PRODH)
ENST00000610940.4:c.*88A>C (PRODH) ENSP00000480347.1:n.*88A>C
NM_001195226.1:c.*88A>C (PRODH) NP_001182155.1:n.*88A>C
NM_016335.4:c.*88A>C (PRODH) NP_057419.4:n.*88A>C
XM_011530278.1:c.*88A>C (PRODH) XP_011528580.1:n.*88A>C
XM_011530279.1:c.*88A>C (PRODH) XP_011528581.1:n.*88A>C
XR_937876.1:n.1958A>C (PRODH)
NM_005675.5:c.*1398T>G (DGCR6) NP_005666.2:n.*1398T>G
NM_001195226.2:c.*88A>C (PRODH) NP_001182155.2:n.*88A>C
NM_016335.5:c.*88A>C (PRODH) NP_057419.5:n.*88A>C
NM_016335.6:c.*88A>C (PRODH) MANE Select NP_057419.5:n.*88A>C