Canonical Allele Identifier: CA410637940

Gene: PRODH DGCR6

Linked Data

• gnomAD v4: 22-18913271-G-T
• MyVariant Identifiers: chr22:g.18900784G>T (hg19) ; chr22:g.18913271G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913271G>T , CM000684.2:g.18913271G>T	GRCh38
NC_000022.10:g.18900784G>T , CM000684.1:g.18900784G>T	GRCh37
NC_000022.9:g.17280784G>T	NCBI36
NG_008226.2:g.28283C>A
NG_009052.1:g.12049G>T
NG_008226.3:g.28283C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1707C>A (PRODH) MANE Select	ENSP00000349577.6:p.Ser569Arg
ENST00000638240.1:c.513+2243G>T	ENSP00000492446.1:n.513+2243G>T
ENST00000313755.9:n.2472C>A (PRODH)
ENST00000334029.6:c.1383C>A (PRODH)	ENSP00000334726.2:p.Ser461Arg
ENST00000357068.10:c.1707C>A (PRODH)	ENSP00000349577.6:p.Ser569Arg
ENST00000420436.5:c.1383C>A (PRODH)	ENSP00000410805.1:p.Ser461Arg
ENST00000429300.5:n.2078C>A (PRODH)
ENST00000482858.5:n.4187C>A (PRODH)
ENST00000483718.5:c.*1913G>T (DGCR6)	ENSP00000467483.1:n.*1913G>T
ENST00000491604.5:n.2616C>A (PRODH)
ENST00000610940.4:c.1707C>A (PRODH)	ENSP00000480347.1:p.Ser569Arg
NM_001195226.1:c.1383C>A (PRODH)	NP_001182155.1:p.Ser461Arg
NM_016335.4:c.1707C>A (PRODH)	NP_057419.4:p.Ser569Arg
XM_011530278.1:c.1134C>A (PRODH)	XP_011528580.1:p.Ser378Arg
XM_011530279.1:c.927C>A (PRODH)	XP_011528581.1:p.Ser309Arg
XR_937876.1:n.1774C>A (PRODH)
NM_005675.5:c.*1582G>T (DGCR6)	NP_005666.2:n.*1582G>T
NM_001195226.2:c.1383C>A (PRODH)	NP_001182155.2:p.Ser461Arg
NM_016335.5:c.1707C>A (PRODH)	NP_057419.5:p.Ser569Arg
NM_016335.6:c.1707C>A (PRODH) MANE Select	NP_057419.5:p.Ser569Arg