Canonical Allele Identifier: CA410649353

Gene: PRODH

Linked Data

• dbSNP Id: rs4819756
• MyVariant Identifiers: chr22:g.18912678A>T (hg19) ; chr22:g.18925165A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18925165A>T , CM000684.2:g.18925165A>T	GRCh38
NC_000022.10:g.18912678A>T , CM000684.1:g.18912678A>T	GRCh37
NC_000022.9:g.17292678A>T	NCBI36
NG_008226.3:g.16389T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357068.11:c.553T>A MANE Select	ENSP00000349577.6:p.Trp185Arg
ENST00000638240.1:c.513+14137A>T	ENSP00000492446.1:n.513+14137A>T
ENST00000334029.6:c.229T>A	ENSP00000334726.2:p.Trp77Arg
ENST00000357068.10:c.553T>A	ENSP00000349577.6:p.Trp185Arg
ENST00000420436.5:c.229T>A	ENSP00000410805.1:p.Trp77Arg
ENST00000438924.5:c.199T>A
ENST00000450579.1:c.76T>A	ENSP00000396806.1:p.Trp26Arg
ENST00000457083.1:c.323T>A
ENST00000482858.5:n.408T>A
ENST00000491604.5:n.561T>A
ENST00000496625.1:n.192T>A
ENST00000610940.4:c.553T>A	ENSP00000480347.1:p.Trp185Arg
XM_011530278.1:c.45T>A	XP_011528580.1:p.Thr15=
XR_937876.1:n.586T>A
NM_001195226.2:c.229T>A	NP_001182155.2:p.Trp77Arg
NM_016335.5:c.553T>A	NP_057419.5:p.Trp185Arg
NM_016335.6:c.553T>A MANE Select	NP_057419.5:p.Trp185Arg