Canonical Allele Identifier: CA2395633567

Gene: PRODH DGCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913229C= , CM000684.2:g.18913229C=	GRCh38
NC_000022.10:g.18900742C= , CM000684.1:g.18900742C=	GRCh37
NC_000022.9:g.17280742C=	NCBI36
NG_008226.2:g.28325G=
NG_009052.1:g.12007C=
NG_008226.3:g.28325G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1749G= (PRODH) MANE Select	ENSP00000349577.6:p.Trp583=
ENST00000638240.1:c.513+2201C=	ENSP00000492446.1:n.513+2201C=
ENST00000313755.9:n.2514G= (PRODH)
ENST00000334029.6:c.1425G= (PRODH)	ENSP00000334726.2:p.Trp475=
ENST00000357068.10:c.1749G= (PRODH)	ENSP00000349577.6:p.Trp583=
ENST00000420436.5:c.1425G= (PRODH)	ENSP00000410805.1:p.Trp475=
ENST00000429300.5:n.2120G= (PRODH)
ENST00000482858.5:n.4229G= (PRODH)
ENST00000483718.5:c.*1871C= (DGCR6)	ENSP00000467483.1:n.*1871C=
ENST00000491604.5:n.2658G= (PRODH)
ENST00000610940.4:c.1749G= (PRODH)	ENSP00000480347.1:p.Trp583=
NM_001195226.1:c.1425G= (PRODH)	NP_001182155.1:p.Trp475=
NM_016335.4:c.1749G= (PRODH)	NP_057419.4:p.Trp583=
XM_011530278.1:c.1176G= (PRODH)	XP_011528580.1:p.Trp392=
XM_011530279.1:c.969G= (PRODH)	XP_011528581.1:p.Trp323=
XR_937876.1:n.1816G= (PRODH)
NM_005675.5:c.*1540C= (DGCR6)	NP_005666.2:n.*1540C=
NM_001195226.2:c.1425G= (PRODH)	NP_001182155.2:p.Trp475=
NM_016335.5:c.1749G= (PRODH)	NP_057419.5:p.Trp583=
NM_016335.6:c.1749G= (PRODH) MANE Select	NP_057419.5:p.Trp583=