Canonical Allele Identifier: CA410642173

Gene: PRODH

Linked Data

• MyVariant Identifiers: chr22:g.18905904C>A (hg19) ; chr22:g.18918391C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18918391C>A , CM000684.2:g.18918391C>A	GRCh38
NC_000022.10:g.18905904C>A , CM000684.1:g.18905904C>A	GRCh37
NC_000022.9:g.17285904C>A	NCBI36
NG_008226.2:g.23163G>T
NG_008226.3:g.23163G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000357068.11:c.1352G>T MANE Select	ENSP00000349577.6:p.Arg451Leu
ENST00000638240.1:c.513+7363C>A	ENSP00000492446.1:n.513+7363C>A
ENST00000313755.9:n.2117G>T
ENST00000334029.6:c.1028G>T	ENSP00000334726.2:p.Arg343Leu
ENST00000357068.10:c.1352G>T	ENSP00000349577.6:p.Arg451Leu
ENST00000420436.5:c.1028G>T	ENSP00000410805.1:p.Arg343Leu
ENST00000429300.5:n.1723G>T
ENST00000482858.5:n.3832G>T
ENST00000491604.5:n.2261G>T
ENST00000609229.1:n.2205G>T
ENST00000610940.4:c.1352G>T	ENSP00000480347.1:p.Arg451Leu
NM_001195226.1:c.1028G>T	NP_001182155.1:p.Arg343Leu
NM_016335.4:c.1352G>T	NP_057419.4:p.Arg451Leu
XM_011530278.1:c.779G>T	XP_011528580.1:p.Arg260Leu
XM_011530279.1:c.572G>T	XP_011528581.1:p.Arg191Leu
XR_937876.1:n.1419G>T
NM_001195226.2:c.1028G>T	NP_001182155.2:p.Arg343Leu
NM_016335.5:c.1352G>T	NP_057419.5:p.Arg451Leu
NM_016335.6:c.1352G>T MANE Select	NP_057419.5:p.Arg451Leu