Canonical Allele Identifier: CA2395633552

Gene: PRODH DGCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913203G= , CM000684.2:g.18913203G=	GRCh38
NC_000022.10:g.18900716G= , CM000684.1:g.18900716G=	GRCh37
NC_000022.9:g.17280716G=	NCBI36
NG_008226.2:g.28351C=
NG_009052.1:g.11981G=
NG_008226.3:g.28351C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1775C= (PRODH) MANE Select	ENSP00000349577.6:p.Thr592=
ENST00000638240.1:c.513+2175G=	ENSP00000492446.1:n.513+2175G=
ENST00000313755.9:n.2540C= (PRODH)
ENST00000334029.6:c.1451C= (PRODH)	ENSP00000334726.2:p.Thr484=
ENST00000357068.10:c.1775C= (PRODH)	ENSP00000349577.6:p.Thr592=
ENST00000420436.5:c.1451C= (PRODH)	ENSP00000410805.1:p.Thr484=
ENST00000429300.5:n.2146C= (PRODH)
ENST00000482858.5:n.4255C= (PRODH)
ENST00000483718.5:c.*1845G= (DGCR6)	ENSP00000467483.1:n.*1845G=
ENST00000491604.5:n.2684C= (PRODH)
ENST00000610940.4:c.1775C= (PRODH)	ENSP00000480347.1:p.Thr592=
NM_001195226.1:c.1451C= (PRODH)	NP_001182155.1:p.Thr484=
NM_016335.4:c.1775C= (PRODH)	NP_057419.4:p.Thr592=
XM_011530278.1:c.1202C= (PRODH)	XP_011528580.1:p.Thr401=
XM_011530279.1:c.995C= (PRODH)	XP_011528581.1:p.Thr332=
XR_937876.1:n.1842C= (PRODH)
NM_005675.5:c.*1514G= (DGCR6)	NP_005666.2:n.*1514G=
NM_001195226.2:c.1451C= (PRODH)	NP_001182155.2:p.Thr484=
NM_016335.5:c.1775C= (PRODH)	NP_057419.5:p.Thr592=
NM_016335.6:c.1775C= (PRODH) MANE Select	NP_057419.5:p.Thr592=