Canonical Allele Identifier: CA410637505

Gene: PRODH DGCR6

Linked Data

• ClinVar Variation Id: 2182392
• ClinVar RCV Id: RCV002610826
• dbSNP Id: rs1157431206
• gnomAD v2: 22-18900698-C-T
• gnomAD v4: 22-18913185-C-T
• MyVariant Identifiers: chr22:g.18900698C>T (hg19) ; chr22:g.18913185C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913185C>T , CM000684.2:g.18913185C>T	GRCh38
NC_000022.10:g.18900698C>T , CM000684.1:g.18900698C>T	GRCh37
NC_000022.9:g.17280698C>T	NCBI36
NG_008226.2:g.28369G>A
NG_009052.1:g.11963C>T
NG_008226.3:g.28369G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1793G>A (PRODH) MANE Select	ENSP00000349577.6:p.Arg598His
ENST00000638240.1:c.513+2157C>T	ENSP00000492446.1:n.513+2157C>T
ENST00000313755.9:n.2558G>A (PRODH)
ENST00000334029.6:c.1469G>A (PRODH)	ENSP00000334726.2:p.Arg490His
ENST00000357068.10:c.1793G>A (PRODH)	ENSP00000349577.6:p.Arg598His
ENST00000420436.5:c.1469G>A (PRODH)	ENSP00000410805.1:p.Arg490His
ENST00000429300.5:n.2164G>A (PRODH)
ENST00000482858.5:n.4273G>A (PRODH)
ENST00000483718.5:c.*1827C>T (DGCR6)	ENSP00000467483.1:n.*1827C>T
ENST00000491604.5:n.2702G>A (PRODH)
ENST00000610940.4:c.1793G>A (PRODH)	ENSP00000480347.1:p.Arg598His
NM_001195226.1:c.1469G>A (PRODH)	NP_001182155.1:p.Arg490His
NM_016335.4:c.1793G>A (PRODH)	NP_057419.4:p.Arg598His
XM_011530278.1:c.1220G>A (PRODH)	XP_011528580.1:p.Arg407His
XM_011530279.1:c.1013G>A (PRODH)	XP_011528581.1:p.Arg338His
XR_937876.1:n.1860G>A (PRODH)
NM_005675.5:c.*1496C>T (DGCR6)	NP_005666.2:n.*1496C>T
NM_001195226.2:c.1469G>A (PRODH)	NP_001182155.2:p.Arg490His
NM_016335.5:c.1793G>A (PRODH)	NP_057419.5:p.Arg598His
NM_016335.6:c.1793G>A (PRODH) MANE Select	NP_057419.5:p.Arg598His