Canonical Allele Identifier: CA410642137

Gene: PRODH

Linked Data

• MyVariant Identifiers: chr22:g.18905896C>T (hg19) ; chr22:g.18918383C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18918383C>T , CM000684.2:g.18918383C>T	GRCh38
NC_000022.10:g.18905896C>T , CM000684.1:g.18905896C>T	GRCh37
NC_000022.9:g.17285896C>T	NCBI36
NG_008226.2:g.23171G>A
NG_008226.3:g.23171G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357068.11:c.1360G>A MANE Select	ENSP00000349577.6:p.Ala454Thr
ENST00000638240.1:c.513+7355C>T	ENSP00000492446.1:n.513+7355C>T
ENST00000313755.9:n.2125G>A
ENST00000334029.6:c.1036G>A	ENSP00000334726.2:p.Ala346Thr
ENST00000357068.10:c.1360G>A	ENSP00000349577.6:p.Ala454Thr
ENST00000420436.5:c.1036G>A	ENSP00000410805.1:p.Ala346Thr
ENST00000429300.5:n.1731G>A
ENST00000482858.5:n.3840G>A
ENST00000491604.5:n.2269G>A
ENST00000609229.1:n.2213G>A
ENST00000610940.4:c.1360G>A	ENSP00000480347.1:p.Ala454Thr
NM_001195226.1:c.1036G>A	NP_001182155.1:p.Ala346Thr
NM_016335.4:c.1360G>A	NP_057419.4:p.Ala454Thr
XM_011530278.1:c.787G>A	XP_011528580.1:p.Ala263Thr
XM_011530279.1:c.580G>A	XP_011528581.1:p.Ala194Thr
XR_937876.1:n.1427G>A
NM_001195226.2:c.1036G>A	NP_001182155.2:p.Ala346Thr
NM_016335.5:c.1360G>A	NP_057419.5:p.Ala454Thr
NM_016335.6:c.1360G>A MANE Select	NP_057419.5:p.Ala454Thr