Canonical Allele Identifier: CA410641923

Gene: PRODH

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1397C>A MANE Select	ENSP00000349577.6:p.Thr466Lys
ENST00000638240.1:c.513+7318G>T	ENSP00000492446.1:n.513+7318G>T
ENST00000313755.9:n.2162C>A
ENST00000334029.6:c.1073C>A	ENSP00000334726.2:p.Thr358Lys
ENST00000357068.10:c.1397C>A	ENSP00000349577.6:p.Thr466Lys
ENST00000420436.5:c.1073C>A	ENSP00000410805.1:p.Thr358Lys
ENST00000429300.5:n.1768C>A
ENST00000482858.5:n.3877C>A
ENST00000491604.5:n.2306C>A
ENST00000609229.1:n.2250C>A
ENST00000610940.4:c.1397C>A	ENSP00000480347.1:p.Thr466Lys
NM_001195226.1:c.1073C>A	NP_001182155.1:p.Thr358Lys
NM_016335.4:c.1397C>A	NP_057419.4:p.Thr466Lys
XM_011530278.1:c.824C>A	XP_011528580.1:p.Thr275Lys
XM_011530279.1:c.617C>A	XP_011528581.1:p.Thr206Lys
XR_937876.1:n.1464C>A
NM_001195226.2:c.1073C>A	NP_001182155.2:p.Thr358Lys
NM_016335.5:c.1397C>A	NP_057419.5:p.Thr466Lys
NM_016335.6:c.1397C>A MANE Select	NP_057419.5:p.Thr466Lys