Canonical Allele Identifier: CA2395634988

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18918329C= , CM000684.2:g.18918329C=	GRCh38
NC_000022.10:g.18905842C= , CM000684.1:g.18905842C=	GRCh37
NC_000022.9:g.17285842C=	NCBI36
NG_008226.2:g.23225G=
NG_008226.3:g.23225G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016335.6:c.1414G= MANE Select	NP_057419.5:p.Ala472=
ENST00000357068.11:c.1414G= MANE Select	ENSP00000349577.6:p.Ala472=
NM_001195226.1:c.1090G=	NP_001182155.1:p.Ala364=
NM_001195226.2:c.1090G=	NP_001182155.2:p.Ala364=
NM_016335.4:c.1414G=	NP_057419.4:p.Ala472=
NM_016335.5:c.1414G=	NP_057419.5:p.Ala472=
ENST00000313755.9:n.2179G=
ENST00000334029.6:c.1090G=	ENSP00000334726.2:p.Ala364=
ENST00000357068.10:c.1414G=	ENSP00000349577.6:p.Ala472=
ENST00000420436.5:c.1090G=	ENSP00000410805.1:p.Ala364=
ENST00000429300.5:n.1785G=
ENST00000482858.5:n.3894G=
ENST00000491604.5:n.2323G=
ENST00000609229.1:n.2267G=
ENST00000610940.4:c.1414G=	ENSP00000480347.1:p.Ala472=
ENST00000638240.1:c.513+7301C=	ENSP00000492446.1:n.513+7301C=
XM_011530278.1:c.841G=	XP_011528580.1:p.Ala281=
XM_011530279.1:c.634G=	XP_011528581.1:p.Ala212=
XR_937876.1:n.1481G=