Canonical Allele Identifier: CA410639193

Gene: PRODH DGCR6

Linked Data

• gnomAD v4: 22-18913513-C-T
• MyVariant Identifiers: chr22:g.18901026C>T (hg19) ; chr22:g.18913513C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913513C>T , CM000684.2:g.18913513C>T	GRCh38
NC_000022.10:g.18901026C>T , CM000684.1:g.18901026C>T	GRCh37
NC_000022.9:g.17281026C>T	NCBI36
NG_008226.2:g.28041G>A
NG_009052.1:g.12291C>T
NG_008226.3:g.28041G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1540G>A (PRODH) MANE Select	ENSP00000349577.6:p.Gly514Ser
ENST00000638240.1:c.513+2485C>T	ENSP00000492446.1:n.513+2485C>T
ENST00000313755.9:n.2305G>A (PRODH)
ENST00000334029.6:c.1216G>A (PRODH)	ENSP00000334726.2:p.Gly406Ser
ENST00000357068.10:c.1540G>A (PRODH)	ENSP00000349577.6:p.Gly514Ser
ENST00000420436.5:c.1216G>A (PRODH)	ENSP00000410805.1:p.Gly406Ser
ENST00000429300.5:n.1911G>A (PRODH)
ENST00000482858.5:n.4020G>A (PRODH)
ENST00000483718.5:c.*2155C>T (DGCR6)	ENSP00000467483.1:n.*2155C>T
ENST00000491604.5:n.2449G>A (PRODH)
ENST00000610940.4:c.1540G>A (PRODH)	ENSP00000480347.1:p.Gly514Ser
NM_001195226.1:c.1216G>A (PRODH)	NP_001182155.1:p.Gly406Ser
NM_016335.4:c.1540G>A (PRODH)	NP_057419.4:p.Gly514Ser
XM_011530278.1:c.967G>A (PRODH)	XP_011528580.1:p.Gly323Ser
XM_011530279.1:c.760G>A (PRODH)	XP_011528581.1:p.Gly254Ser
XR_937876.1:n.1607G>A (PRODH)
NM_005675.5:c.*1824C>T (DGCR6)	NP_005666.2:n.*1824C>T
NM_001195226.2:c.1216G>A (PRODH)	NP_001182155.2:p.Gly406Ser
NM_016335.5:c.1540G>A (PRODH)	NP_057419.5:p.Gly514Ser
NM_016335.6:c.1540G>A (PRODH) MANE Select	NP_057419.5:p.Gly514Ser