Canonical Allele Identifier: CA1024068804

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913104T>G , CM000684.2:g.18913104T>G GRCh38
NC_000022.10:g.18900617T>G , CM000684.1:g.18900617T>G GRCh37
NC_000022.9:g.17280617T>G NCBI36
NG_008226.2:g.28450A>C
NG_009052.1:g.11882T>G
NG_008226.3:g.28450A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*71A>C (PRODH) MANE Select ENSP00000349577.6:n.*71A>C
ENST00000638240.1:c.513+2076T>G ENSP00000492446.1:n.513+2076T>G
ENST00000313755.9:n.2639A>C (PRODH)
ENST00000334029.6:c.*71A>C (PRODH) ENSP00000334726.2:n.*71A>C
ENST00000357068.10:c.*71A>C (PRODH) ENSP00000349577.6:n.*71A>C
ENST00000420436.5:c.*71A>C (PRODH) ENSP00000410805.1:n.*71A>C
ENST00000429300.5:n.2245A>C (PRODH)
ENST00000482858.5:n.4354A>C (PRODH)
ENST00000483718.5:c.*1746T>G (DGCR6) ENSP00000467483.1:n.*1746T>G
ENST00000491604.5:n.2783A>C (PRODH)
ENST00000610940.4:c.*71A>C (PRODH) ENSP00000480347.1:n.*71A>C
NM_001195226.1:c.*71A>C (PRODH) NP_001182155.1:n.*71A>C
NM_016335.4:c.*71A>C (PRODH) NP_057419.4:n.*71A>C
XM_011530278.1:c.*71A>C (PRODH) XP_011528580.1:n.*71A>C
XM_011530279.1:c.*71A>C (PRODH) XP_011528581.1:n.*71A>C
XR_937876.1:n.1941A>C (PRODH)
NM_005675.5:c.*1415T>G (DGCR6) NP_005666.2:n.*1415T>G
NM_001195226.2:c.*71A>C (PRODH) NP_001182155.2:n.*71A>C
NM_016335.5:c.*71A>C (PRODH) NP_057419.5:n.*71A>C
NM_016335.6:c.*71A>C (PRODH) MANE Select NP_057419.5:n.*71A>C