Canonical Allele Identifier: CA512936880

Gene: PRODH DGCR6

Linked Data

• gnomAD v4: 22-18913322-G-T
• MyVariant Identifiers: chr22:g.18900835G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913322G>T , CM000684.2:g.18913322G>T	GRCh38
NC_000022.10:g.18900835G>T , CM000684.1:g.18900835G>T	GRCh37
NC_000022.9:g.17280835G>T	NCBI36
NG_008226.2:g.28232C>A
NG_009052.1:g.12100G>T
NG_008226.3:g.28232C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1656C>A (PRODH) MANE Select	ENSP00000349577.6:p.Gly552=
ENST00000638240.1:c.513+2294G>T	ENSP00000492446.1:n.513+2294G>T
ENST00000313755.9:n.2421C>A (PRODH)
ENST00000334029.6:c.1332C>A (PRODH)	ENSP00000334726.2:p.Gly444=
ENST00000357068.10:c.1656C>A (PRODH)	ENSP00000349577.6:p.Gly552=
ENST00000420436.5:c.1332C>A (PRODH)	ENSP00000410805.1:p.Gly444=
ENST00000429300.5:n.2027C>A (PRODH)
ENST00000482858.5:n.4136C>A (PRODH)
ENST00000483718.5:c.*1964G>T (DGCR6)	ENSP00000467483.1:n.*1964G>T
ENST00000491604.5:n.2565C>A (PRODH)
ENST00000610940.4:c.1656C>A (PRODH)	ENSP00000480347.1:p.Gly552=
NM_001195226.1:c.1332C>A (PRODH)	NP_001182155.1:p.Gly444=
NM_016335.4:c.1656C>A (PRODH)	NP_057419.4:p.Gly552=
XM_011530278.1:c.1083C>A (PRODH)	XP_011528580.1:p.Gly361=
XM_011530279.1:c.876C>A (PRODH)	XP_011528581.1:p.Gly292=
XR_937876.1:n.1723C>A (PRODH)
NM_005675.5:c.*1633G>T (DGCR6)	NP_005666.2:n.*1633G>T
NM_001195226.2:c.1332C>A (PRODH)	NP_001182155.2:p.Gly444=
NM_016335.5:c.1656C>A (PRODH)	NP_057419.5:p.Gly552=
NM_016335.6:c.1656C>A (PRODH) MANE Select	NP_057419.5:p.Gly552=