Canonical Allele Identifier: CA2395633501

Linked Data

dbSNP Id: rs2081916859

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913098A>T , CM000684.2:g.18913098A>T GRCh38
NC_000022.10:g.18900611A>T , CM000684.1:g.18900611A>T GRCh37
NC_000022.9:g.17280611A>T NCBI36
NG_008226.2:g.28456T>A
NG_009052.1:g.11876A>T
NG_008226.3:g.28456T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*77T>A (PRODH) MANE Select ENSP00000349577.6:n.*77T>A
ENST00000638240.1:c.513+2070A>T ENSP00000492446.1:n.513+2070A>T
ENST00000313755.9:n.2645T>A (PRODH)
ENST00000334029.6:c.*77T>A (PRODH) ENSP00000334726.2:n.*77T>A
ENST00000357068.10:c.*77T>A (PRODH) ENSP00000349577.6:n.*77T>A
ENST00000420436.5:c.*77T>A (PRODH) ENSP00000410805.1:n.*77T>A
ENST00000429300.5:n.2251T>A (PRODH)
ENST00000482858.5:n.4360T>A (PRODH)
ENST00000483718.5:c.*1740A>T (DGCR6) ENSP00000467483.1:n.*1740A>T
ENST00000491604.5:n.2789T>A (PRODH)
ENST00000610940.4:c.*77T>A (PRODH) ENSP00000480347.1:n.*77T>A
NM_001195226.1:c.*77T>A (PRODH) NP_001182155.1:n.*77T>A
NM_016335.4:c.*77T>A (PRODH) NP_057419.4:n.*77T>A
XM_011530278.1:c.*77T>A (PRODH) XP_011528580.1:n.*77T>A
XM_011530279.1:c.*77T>A (PRODH) XP_011528581.1:n.*77T>A
XR_937876.1:n.1947T>A (PRODH)
NM_005675.5:c.*1409A>T (DGCR6) NP_005666.2:n.*1409A>T
NM_001195226.2:c.*77T>A (PRODH) NP_001182155.2:n.*77T>A
NM_016335.5:c.*77T>A (PRODH) NP_057419.5:n.*77T>A
NM_016335.6:c.*77T>A (PRODH) MANE Select NP_057419.5:n.*77T>A