Canonical Allele Identifier: CA410637570

Gene: PRODH DGCR6

Linked Data

• gnomAD v4: 22-18913198-T-C
• MyVariant Identifiers: chr22:g.18900711T>C (hg19) ; chr22:g.18913198T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913198T>C , CM000684.2:g.18913198T>C	GRCh38
NC_000022.10:g.18900711T>C , CM000684.1:g.18900711T>C	GRCh37
NC_000022.9:g.17280711T>C	NCBI36
NG_008226.2:g.28356A>G
NG_009052.1:g.11976T>C
NG_008226.3:g.28356A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1780A>G (PRODH) MANE Select	ENSP00000349577.6:p.Asn594Asp
ENST00000638240.1:c.513+2170T>C	ENSP00000492446.1:n.513+2170T>C
ENST00000313755.9:n.2545A>G (PRODH)
ENST00000334029.6:c.1456A>G (PRODH)	ENSP00000334726.2:p.Asn486Asp
ENST00000357068.10:c.1780A>G (PRODH)	ENSP00000349577.6:p.Asn594Asp
ENST00000420436.5:c.1456A>G (PRODH)	ENSP00000410805.1:p.Asn486Asp
ENST00000429300.5:n.2151A>G (PRODH)
ENST00000482858.5:n.4260A>G (PRODH)
ENST00000483718.5:c.*1840T>C (DGCR6)	ENSP00000467483.1:n.*1840T>C
ENST00000491604.5:n.2689A>G (PRODH)
ENST00000610940.4:c.1780A>G (PRODH)	ENSP00000480347.1:p.Asn594Asp
NM_001195226.1:c.1456A>G (PRODH)	NP_001182155.1:p.Asn486Asp
NM_016335.4:c.1780A>G (PRODH)	NP_057419.4:p.Asn594Asp
XM_011530278.1:c.1207A>G (PRODH)	XP_011528580.1:p.Asn403Asp
XM_011530279.1:c.1000A>G (PRODH)	XP_011528581.1:p.Asn334Asp
XR_937876.1:n.1847A>G (PRODH)
NM_005675.5:c.*1509T>C (DGCR6)	NP_005666.2:n.*1509T>C
NM_001195226.2:c.1456A>G (PRODH)	NP_001182155.2:p.Asn486Asp
NM_016335.5:c.1780A>G (PRODH)	NP_057419.5:p.Asn594Asp
NM_016335.6:c.1780A>G (PRODH) MANE Select	NP_057419.5:p.Asn594Asp