Canonical Allele Identifier: CA2395633553

Gene: PRODH DGCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913206C= , CM000684.2:g.18913206C=	GRCh38
NC_000022.10:g.18900719C= , CM000684.1:g.18900719C=	GRCh37
NC_000022.9:g.17280719C=	NCBI36
NG_008226.2:g.28348G=
NG_009052.1:g.11984C=
NG_008226.3:g.28348G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1772G= (PRODH) MANE Select	ENSP00000349577.6:p.Arg591=
ENST00000638240.1:c.513+2178C=	ENSP00000492446.1:n.513+2178C=
ENST00000313755.9:n.2537G= (PRODH)
ENST00000334029.6:c.1448G= (PRODH)	ENSP00000334726.2:p.Arg483=
ENST00000357068.10:c.1772G= (PRODH)	ENSP00000349577.6:p.Arg591=
ENST00000420436.5:c.1448G= (PRODH)	ENSP00000410805.1:p.Arg483=
ENST00000429300.5:n.2143G= (PRODH)
ENST00000482858.5:n.4252G= (PRODH)
ENST00000483718.5:c.*1848C= (DGCR6)	ENSP00000467483.1:n.*1848C=
ENST00000491604.5:n.2681G= (PRODH)
ENST00000610940.4:c.1772G= (PRODH)	ENSP00000480347.1:p.Arg591=
NM_001195226.1:c.1448G= (PRODH)	NP_001182155.1:p.Arg483=
NM_016335.4:c.1772G= (PRODH)	NP_057419.4:p.Arg591=
XM_011530278.1:c.1199G= (PRODH)	XP_011528580.1:p.Arg400=
XM_011530279.1:c.992G= (PRODH)	XP_011528581.1:p.Arg331=
XR_937876.1:n.1839G= (PRODH)
NM_005675.5:c.*1517C= (DGCR6)	NP_005666.2:n.*1517C=
NM_001195226.2:c.1448G= (PRODH)	NP_001182155.2:p.Arg483=
NM_016335.5:c.1772G= (PRODH)	NP_057419.5:p.Arg591=
NM_016335.6:c.1772G= (PRODH) MANE Select	NP_057419.5:p.Arg591=