Canonical Allele Identifier: CA2395634999

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18918346G= , CM000684.2:g.18918346G=	GRCh38
NC_000022.10:g.18905859G= , CM000684.1:g.18905859G=	GRCh37
NC_000022.9:g.17285859G=	NCBI36
NG_008226.2:g.23208C=
NG_008226.3:g.23208C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016335.6:c.1397C= MANE Select	NP_057419.5:p.Thr466=
ENST00000357068.11:c.1397C= MANE Select	ENSP00000349577.6:p.Thr466=
NM_001195226.1:c.1073C=	NP_001182155.1:p.Thr358=
NM_001195226.2:c.1073C=	NP_001182155.2:p.Thr358=
NM_016335.4:c.1397C=	NP_057419.4:p.Thr466=
NM_016335.5:c.1397C=	NP_057419.5:p.Thr466=
ENST00000313755.9:n.2162C=
ENST00000334029.6:c.1073C=	ENSP00000334726.2:p.Thr358=
ENST00000357068.10:c.1397C=	ENSP00000349577.6:p.Thr466=
ENST00000420436.5:c.1073C=	ENSP00000410805.1:p.Thr358=
ENST00000429300.5:n.1768C=
ENST00000482858.5:n.3877C=
ENST00000491604.5:n.2306C=
ENST00000609229.1:n.2250C=
ENST00000610940.4:c.1397C=	ENSP00000480347.1:p.Thr466=
ENST00000638240.1:c.513+7318G=	ENSP00000492446.1:n.513+7318G=
XM_011530278.1:c.824C=	XP_011528580.1:p.Thr275=
XM_011530279.1:c.617C=	XP_011528581.1:p.Thr206=
XR_937876.1:n.1464C=