Canonical Allele Identifier: CA410642119

Gene: PRODH

Linked Data

• gnomAD v4: 22-18918380-C-T
• MyVariant Identifiers: chr22:g.18905893C>T (hg19) ; chr22:g.18918380C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18918380C>T , CM000684.2:g.18918380C>T	GRCh38
NC_000022.10:g.18905893C>T , CM000684.1:g.18905893C>T	GRCh37
NC_000022.9:g.17285893C>T	NCBI36
NG_008226.2:g.23174G>A
NG_008226.3:g.23174G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357068.11:c.1363G>A MANE Select	ENSP00000349577.6:p.Ala455Thr
ENST00000638240.1:c.513+7352C>T	ENSP00000492446.1:n.513+7352C>T
ENST00000313755.9:n.2128G>A
ENST00000334029.6:c.1039G>A	ENSP00000334726.2:p.Ala347Thr
ENST00000357068.10:c.1363G>A	ENSP00000349577.6:p.Ala455Thr
ENST00000420436.5:c.1039G>A	ENSP00000410805.1:p.Ala347Thr
ENST00000429300.5:n.1734G>A
ENST00000482858.5:n.3843G>A
ENST00000491604.5:n.2272G>A
ENST00000609229.1:n.2216G>A
ENST00000610940.4:c.1363G>A	ENSP00000480347.1:p.Ala455Thr
NM_001195226.1:c.1039G>A	NP_001182155.1:p.Ala347Thr
NM_016335.4:c.1363G>A	NP_057419.4:p.Ala455Thr
XM_011530278.1:c.790G>A	XP_011528580.1:p.Ala264Thr
XM_011530279.1:c.583G>A	XP_011528581.1:p.Ala195Thr
XR_937876.1:n.1430G>A
NM_001195226.2:c.1039G>A	NP_001182155.2:p.Ala347Thr
NM_016335.5:c.1363G>A	NP_057419.5:p.Ala455Thr
NM_016335.6:c.1363G>A MANE Select	NP_057419.5:p.Ala455Thr