Canonical Allele Identifier: CA2655228909

Gene: PRODH DGCR6

Linked Data

• gnomAD v4: 22-18913165-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913165C>A , CM000684.2:g.18913165C>A	GRCh38
NC_000022.10:g.18900678C>A , CM000684.1:g.18900678C>A	GRCh37
NC_000022.9:g.17280678C>A	NCBI36
NG_008226.2:g.28389G>T
NG_009052.1:g.11943C>A
NG_008226.3:g.28389G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.*10G>T (PRODH) MANE Select	ENSP00000349577.6:n.*10G>T
ENST00000638240.1:c.513+2137C>A	ENSP00000492446.1:n.513+2137C>A
ENST00000313755.9:n.2578G>T (PRODH)
ENST00000334029.6:c.*10G>T (PRODH)	ENSP00000334726.2:n.*10G>T
ENST00000357068.10:c.*10G>T (PRODH)	ENSP00000349577.6:n.*10G>T
ENST00000420436.5:c.*10G>T (PRODH)	ENSP00000410805.1:n.*10G>T
ENST00000429300.5:n.2184G>T (PRODH)
ENST00000482858.5:n.4293G>T (PRODH)
ENST00000483718.5:c.*1807C>A (DGCR6)	ENSP00000467483.1:n.*1807C>A
ENST00000491604.5:n.2722G>T (PRODH)
ENST00000610940.4:c.*10G>T (PRODH)	ENSP00000480347.1:n.*10G>T
NM_001195226.1:c.*10G>T (PRODH)	NP_001182155.1:n.*10G>T
NM_016335.4:c.*10G>T (PRODH)	NP_057419.4:n.*10G>T
XM_011530278.1:c.*10G>T (PRODH)	XP_011528580.1:n.*10G>T
XM_011530279.1:c.*10G>T (PRODH)	XP_011528581.1:n.*10G>T
XR_937876.1:n.1880G>T (PRODH)
NM_005675.5:c.*1476C>A (DGCR6)	NP_005666.2:n.*1476C>A
NM_001195226.2:c.*10G>T (PRODH)	NP_001182155.2:n.*10G>T
NM_016335.5:c.*10G>T (PRODH)	NP_057419.5:n.*10G>T
NM_016335.6:c.*10G>T (PRODH) MANE Select	NP_057419.5:n.*10G>T