Canonical Allele Identifier: CA2395635021

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18918386G= , CM000684.2:g.18918386G=	GRCh38
NC_000022.10:g.18905899G= , CM000684.1:g.18905899G=	GRCh37
NC_000022.9:g.17285899G=	NCBI36
NG_008226.2:g.23168C=
NG_008226.3:g.23168C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016335.6:c.1357C= MANE Select	NP_057419.5:p.Arg453=
ENST00000357068.11:c.1357C= MANE Select	ENSP00000349577.6:p.Arg453=
NM_001195226.1:c.1033C=	NP_001182155.1:p.Arg345=
NM_001195226.2:c.1033C=	NP_001182155.2:p.Arg345=
NM_016335.4:c.1357C=	NP_057419.4:p.Arg453=
NM_016335.5:c.1357C=	NP_057419.5:p.Arg453=
ENST00000313755.9:n.2122C=
ENST00000334029.6:c.1033C=	ENSP00000334726.2:p.Arg345=
ENST00000357068.10:c.1357C=	ENSP00000349577.6:p.Arg453=
ENST00000420436.5:c.1033C=	ENSP00000410805.1:p.Arg345=
ENST00000429300.5:n.1728C=
ENST00000482858.5:n.3837C=
ENST00000491604.5:n.2266C=
ENST00000609229.1:n.2210C=
ENST00000610940.4:c.1357C=	ENSP00000480347.1:p.Arg453=
ENST00000638240.1:c.513+7358G=	ENSP00000492446.1:n.513+7358G=
XM_011530278.1:c.784C=	XP_011528580.1:p.Arg262=
XM_011530279.1:c.577C=	XP_011528581.1:p.Arg193=
XR_937876.1:n.1424C=