Canonical Allele Identifier: CA410637507

Gene: PRODH DGCR6

Linked Data

• gnomAD v4: 22-18913186-G-T
• MyVariant Identifiers: chr22:g.18900699G>T (hg19) ; chr22:g.18913186G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913186G>T , CM000684.2:g.18913186G>T	GRCh38
NC_000022.10:g.18900699G>T , CM000684.1:g.18900699G>T	GRCh37
NC_000022.9:g.17280699G>T	NCBI36
NG_008226.2:g.28368C>A
NG_009052.1:g.11964G>T
NG_008226.3:g.28368C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1792C>A (PRODH) MANE Select	ENSP00000349577.6:p.Arg598Ser
ENST00000638240.1:c.513+2158G>T	ENSP00000492446.1:n.513+2158G>T
ENST00000313755.9:n.2557C>A (PRODH)
ENST00000334029.6:c.1468C>A (PRODH)	ENSP00000334726.2:p.Arg490Ser
ENST00000357068.10:c.1792C>A (PRODH)	ENSP00000349577.6:p.Arg598Ser
ENST00000420436.5:c.1468C>A (PRODH)	ENSP00000410805.1:p.Arg490Ser
ENST00000429300.5:n.2163C>A (PRODH)
ENST00000482858.5:n.4272C>A (PRODH)
ENST00000483718.5:c.*1828G>T (DGCR6)	ENSP00000467483.1:n.*1828G>T
ENST00000491604.5:n.2701C>A (PRODH)
ENST00000610940.4:c.1792C>A (PRODH)	ENSP00000480347.1:p.Arg598Ser
NM_001195226.1:c.1468C>A (PRODH)	NP_001182155.1:p.Arg490Ser
NM_016335.4:c.1792C>A (PRODH)	NP_057419.4:p.Arg598Ser
XM_011530278.1:c.1219C>A (PRODH)	XP_011528580.1:p.Arg407Ser
XM_011530279.1:c.1012C>A (PRODH)	XP_011528581.1:p.Arg338Ser
XR_937876.1:n.1859C>A (PRODH)
NM_005675.5:c.*1497G>T (DGCR6)	NP_005666.2:n.*1497G>T
NM_001195226.2:c.1468C>A (PRODH)	NP_001182155.2:p.Arg490Ser
NM_016335.5:c.1792C>A (PRODH)	NP_057419.5:p.Arg598Ser
NM_016335.6:c.1792C>A (PRODH) MANE Select	NP_057419.5:p.Arg598Ser