Canonical Allele Identifier: CA658658903

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18925165A= , CM000684.2:g.18925165A=	GRCh38
NC_000022.10:g.18912678A= , CM000684.1:g.18912678A=	GRCh37
NC_000022.9:g.17292678A=	NCBI36
NG_008226.3:g.16389T=

Transcript Alleles

HGVS	Amino-acid Change
NM_016335.6:c.553T= MANE Select	NP_057419.5:p.Trp185=
ENST00000357068.11:c.553T= MANE Select	ENSP00000349577.6:p.Trp185=
NM_001195226.2:c.229T=	NP_001182155.2:p.Trp77=
NM_016335.5:c.553T=	NP_057419.5:p.Trp185=
ENST00000334029.6:c.229T=	ENSP00000334726.2:p.Trp77=
ENST00000357068.10:c.553T=	ENSP00000349577.6:p.Trp185=
ENST00000420436.5:c.229T=	ENSP00000410805.1:p.Trp77=
ENST00000438924.5:c.199T=
ENST00000450579.1:c.76T=	ENSP00000396806.1:p.Trp26=
ENST00000457083.1:c.323T=
ENST00000482858.5:n.408T=
ENST00000491604.5:n.561T=
ENST00000496625.1:n.192T=
ENST00000610940.4:c.553T=	ENSP00000480347.1:p.Trp185=
ENST00000638240.1:c.513+14137A=	ENSP00000492446.1:n.513+14137A=
XM_011530278.1:c.45T=	XP_011528580.1:p.Thr15=
XR_937876.1:n.586T=