Canonical Allele Identifier: CA2395634663

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18917482A>T , CM000684.2:g.18917482A>T	GRCh38
NC_000022.10:g.18904995A>T , CM000684.1:g.18904995A>T	GRCh37
NC_000022.9:g.17284995A>T	NCBI36
NG_008226.2:g.24072T>A
NG_008226.3:g.24072T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016335.6:c.1428-494T>A MANE Select	NP_057419.5:n.1428-494T>A
ENST00000357068.11:c.1428-494T>A MANE Select	ENSP00000349577.6:n.1428-494T>A
NM_001195226.1:c.1104-494T>A	NP_001182155.1:n.1104-494T>A
NM_001195226.2:c.1104-494T>A	NP_001182155.2:n.1104-494T>A
NM_016335.4:c.1428-494T>A	NP_057419.4:n.1428-494T>A
NM_016335.5:c.1428-494T>A	NP_057419.5:n.1428-494T>A
ENST00000313755.9:n.2193-494T>A
ENST00000334029.6:c.1104-494T>A	ENSP00000334726.2:n.1104-494T>A
ENST00000357068.10:c.1428-494T>A	ENSP00000349577.6:n.1428-494T>A
ENST00000420436.5:c.1104-494T>A	ENSP00000410805.1:n.1104-494T>A
ENST00000429300.5:n.1799-494T>A
ENST00000482858.5:n.3908-494T>A
ENST00000491604.5:n.2337-494T>A
ENST00000609229.1:n.2281-494T>A
ENST00000610940.4:c.1428-494T>A	ENSP00000480347.1:n.1428-494T>A
ENST00000638240.1:c.513+6454A>T	ENSP00000492446.1:n.513+6454A>T
XM_011530278.1:c.855-494T>A	XP_011528580.1:n.855-494T>A
XM_011530279.1:c.648-494T>A	XP_011528581.1:n.648-494T>A
XR_937876.1:n.1495-494T>A