Canonical Allele Identifier: CA2395633575

Gene: PRODH DGCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913246C= , CM000684.2:g.18913246C=	GRCh38
NC_000022.10:g.18900759C= , CM000684.1:g.18900759C=	GRCh37
NC_000022.9:g.17280759C=	NCBI36
NG_008226.2:g.28308G=
NG_009052.1:g.12024C=
NG_008226.3:g.28308G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1732G= (PRODH) MANE Select	ENSP00000349577.6:p.Glu578=
ENST00000638240.1:c.513+2218C=	ENSP00000492446.1:n.513+2218C=
ENST00000313755.9:n.2497G= (PRODH)
ENST00000334029.6:c.1408G= (PRODH)	ENSP00000334726.2:p.Glu470=
ENST00000357068.10:c.1732G= (PRODH)	ENSP00000349577.6:p.Glu578=
ENST00000420436.5:c.1408G= (PRODH)	ENSP00000410805.1:p.Glu470=
ENST00000429300.5:n.2103G= (PRODH)
ENST00000482858.5:n.4212G= (PRODH)
ENST00000483718.5:c.*1888C= (DGCR6)	ENSP00000467483.1:n.*1888C=
ENST00000491604.5:n.2641G= (PRODH)
ENST00000610940.4:c.1732G= (PRODH)	ENSP00000480347.1:p.Glu578=
NM_001195226.1:c.1408G= (PRODH)	NP_001182155.1:p.Glu470=
NM_016335.4:c.1732G= (PRODH)	NP_057419.4:p.Glu578=
XM_011530278.1:c.1159G= (PRODH)	XP_011528580.1:p.Glu387=
XM_011530279.1:c.952G= (PRODH)	XP_011528581.1:p.Glu318=
XR_937876.1:n.1799G= (PRODH)
NM_005675.5:c.*1557C= (DGCR6)	NP_005666.2:n.*1557C=
NM_001195226.2:c.1408G= (PRODH)	NP_001182155.2:p.Glu470=
NM_016335.5:c.1732G= (PRODH)	NP_057419.5:p.Glu578=
NM_016335.6:c.1732G= (PRODH) MANE Select	NP_057419.5:p.Glu578=