Canonical Allele Identifier: CA2655228879

Gene: PRODH DGCR6

Linked Data

• gnomAD v4: 22-18913134-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913134G>T , CM000684.2:g.18913134G>T	GRCh38
NC_000022.10:g.18900647G>T , CM000684.1:g.18900647G>T	GRCh37
NC_000022.9:g.17280647G>T	NCBI36
NG_008226.2:g.28420C>A
NG_009052.1:g.11912G>T
NG_008226.3:g.28420C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.*41C>A (PRODH) MANE Select	ENSP00000349577.6:n.*41C>A
ENST00000638240.1:c.513+2106G>T	ENSP00000492446.1:n.513+2106G>T
ENST00000313755.9:n.2609C>A (PRODH)
ENST00000334029.6:c.*41C>A (PRODH)	ENSP00000334726.2:n.*41C>A
ENST00000357068.10:c.*41C>A (PRODH)	ENSP00000349577.6:n.*41C>A
ENST00000420436.5:c.*41C>A (PRODH)	ENSP00000410805.1:n.*41C>A
ENST00000429300.5:n.2215C>A (PRODH)
ENST00000482858.5:n.4324C>A (PRODH)
ENST00000483718.5:c.*1776G>T (DGCR6)	ENSP00000467483.1:n.*1776G>T
ENST00000491604.5:n.2753C>A (PRODH)
ENST00000610940.4:c.*41C>A (PRODH)	ENSP00000480347.1:n.*41C>A
NM_001195226.1:c.*41C>A (PRODH)	NP_001182155.1:n.*41C>A
NM_016335.4:c.*41C>A (PRODH)	NP_057419.4:n.*41C>A
XM_011530278.1:c.*41C>A (PRODH)	XP_011528580.1:n.*41C>A
XM_011530279.1:c.*41C>A (PRODH)	XP_011528581.1:n.*41C>A
XR_937876.1:n.1911C>A (PRODH)
NM_005675.5:c.*1445G>T (DGCR6)	NP_005666.2:n.*1445G>T
NM_001195226.2:c.*41C>A (PRODH)	NP_001182155.2:n.*41C>A
NM_016335.5:c.*41C>A (PRODH)	NP_057419.5:n.*41C>A
NM_016335.6:c.*41C>A (PRODH) MANE Select	NP_057419.5:n.*41C>A