Canonical Allele Identifier: CA410637841

Gene: PRODH DGCR6

Linked Data

• MyVariant Identifiers: chr22:g.18900770C>G (hg19) ; chr22:g.18913257C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913257C>G , CM000684.2:g.18913257C>G	GRCh38
NC_000022.10:g.18900770C>G , CM000684.1:g.18900770C>G	GRCh37
NC_000022.9:g.17280770C>G	NCBI36
NG_008226.2:g.28297G>C
NG_009052.1:g.12035C>G
NG_008226.3:g.28297G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1721G>C (PRODH) MANE Select	ENSP00000349577.6:p.Gly574Ala
ENST00000638240.1:c.513+2229C>G	ENSP00000492446.1:n.513+2229C>G
ENST00000313755.9:n.2486G>C (PRODH)
ENST00000334029.6:c.1397G>C (PRODH)	ENSP00000334726.2:p.Gly466Ala
ENST00000357068.10:c.1721G>C (PRODH)	ENSP00000349577.6:p.Gly574Ala
ENST00000420436.5:c.1397G>C (PRODH)	ENSP00000410805.1:p.Gly466Ala
ENST00000429300.5:n.2092G>C (PRODH)
ENST00000482858.5:n.4201G>C (PRODH)
ENST00000483718.5:c.*1899C>G (DGCR6)	ENSP00000467483.1:n.*1899C>G
ENST00000491604.5:n.2630G>C (PRODH)
ENST00000610940.4:c.1721G>C (PRODH)	ENSP00000480347.1:p.Gly574Ala
NM_001195226.1:c.1397G>C (PRODH)	NP_001182155.1:p.Gly466Ala
NM_016335.4:c.1721G>C (PRODH)	NP_057419.4:p.Gly574Ala
XM_011530278.1:c.1148G>C (PRODH)	XP_011528580.1:p.Gly383Ala
XM_011530279.1:c.941G>C (PRODH)	XP_011528581.1:p.Gly314Ala
XR_937876.1:n.1788G>C (PRODH)
NM_005675.5:c.*1568C>G (DGCR6)	NP_005666.2:n.*1568C>G
NM_001195226.2:c.1397G>C (PRODH)	NP_001182155.2:p.Gly466Ala
NM_016335.5:c.1721G>C (PRODH)	NP_057419.5:p.Gly574Ala
NM_016335.6:c.1721G>C (PRODH) MANE Select	NP_057419.5:p.Gly574Ala