Canonical Allele Identifier: CA2395635056

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18918451C= , CM000684.2:g.18918451C=	GRCh38
NC_000022.10:g.18905964C= , CM000684.1:g.18905964C=	GRCh37
NC_000022.9:g.17285964C=	NCBI36
NG_008226.2:g.23103G=
NG_008226.3:g.23103G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016335.6:c.1292G= MANE Select	NP_057419.5:p.Arg431=
ENST00000357068.11:c.1292G= MANE Select	ENSP00000349577.6:p.Arg431=
NM_001195226.1:c.968G=	NP_001182155.1:p.Arg323=
NM_001195226.2:c.968G=	NP_001182155.2:p.Arg323=
NM_016335.4:c.1292G=	NP_057419.4:p.Arg431=
NM_016335.5:c.1292G=	NP_057419.5:p.Arg431=
ENST00000313755.9:n.2057G=
ENST00000334029.6:c.968G=	ENSP00000334726.2:p.Arg323=
ENST00000357068.10:c.1292G=	ENSP00000349577.6:p.Arg431=
ENST00000420436.5:c.968G=	ENSP00000410805.1:p.Arg323=
ENST00000429300.5:n.1663G=
ENST00000482858.5:n.3772G=
ENST00000491604.5:n.2201G=
ENST00000609229.1:n.2145G=
ENST00000610940.4:c.1292G=	ENSP00000480347.1:p.Arg431=
ENST00000638240.1:c.513+7423C=	ENSP00000492446.1:n.513+7423C=
XM_011530278.1:c.719G=	XP_011528580.1:p.Arg240=
XM_011530279.1:c.512G=	XP_011528581.1:p.Arg171=
XR_937876.1:n.1359G=