Canonical Allele Identifier: CA410639027

Gene: PRODH DGCR6

Linked Data

• MyVariant Identifiers: chr22:g.18900999A>C (hg19) ; chr22:g.18913486A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913486A>C , CM000684.2:g.18913486A>C	GRCh38
NC_000022.10:g.18900999A>C , CM000684.1:g.18900999A>C	GRCh37
NC_000022.9:g.17280999A>C	NCBI36
NG_008226.2:g.28068T>G
NG_009052.1:g.12264A>C
NG_008226.3:g.28068T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1567T>G (PRODH) MANE Select	ENSP00000349577.6:p.Tyr523Asp
ENST00000638240.1:c.513+2458A>C	ENSP00000492446.1:n.513+2458A>C
ENST00000313755.9:n.2332T>G (PRODH)
ENST00000334029.6:c.1243T>G (PRODH)	ENSP00000334726.2:p.Tyr415Asp
ENST00000357068.10:c.1567T>G (PRODH)	ENSP00000349577.6:p.Tyr523Asp
ENST00000420436.5:c.1243T>G (PRODH)	ENSP00000410805.1:p.Tyr415Asp
ENST00000429300.5:n.1938T>G (PRODH)
ENST00000482858.5:n.4047T>G (PRODH)
ENST00000483718.5:c.*2128A>C (DGCR6)	ENSP00000467483.1:n.*2128A>C
ENST00000491604.5:n.2476T>G (PRODH)
ENST00000610940.4:c.1567T>G (PRODH)	ENSP00000480347.1:p.Tyr523Asp
NM_001195226.1:c.1243T>G (PRODH)	NP_001182155.1:p.Tyr415Asp
NM_016335.4:c.1567T>G (PRODH)	NP_057419.4:p.Tyr523Asp
XM_011530278.1:c.994T>G (PRODH)	XP_011528580.1:p.Tyr332Asp
XM_011530279.1:c.787T>G (PRODH)	XP_011528581.1:p.Tyr263Asp
XR_937876.1:n.1634T>G (PRODH)
NM_005675.5:c.*1797A>C (DGCR6)	NP_005666.2:n.*1797A>C
NM_001195226.2:c.1243T>G (PRODH)	NP_001182155.2:p.Tyr415Asp
NM_016335.5:c.1567T>G (PRODH)	NP_057419.5:p.Tyr523Asp
NM_016335.6:c.1567T>G (PRODH) MANE Select	NP_057419.5:p.Tyr523Asp