Canonical Allele Identifier: CA410638817

Gene: PRODH DGCR6

Linked Data

• dbSNP Id: rs1379632175
• gnomAD v2: 22-18900974-C-T
• MyVariant Identifiers: chr22:g.18900974C>T (hg19) ; chr22:g.18913461C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913461C>T , CM000684.2:g.18913461C>T	GRCh38
NC_000022.10:g.18900974C>T , CM000684.1:g.18900974C>T	GRCh37
NC_000022.9:g.17280974C>T	NCBI36
NG_008226.2:g.28093G>A
NG_009052.1:g.12239C>T
NG_008226.3:g.28093G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1592G>A (PRODH) MANE Select	ENSP00000349577.6:p.Cys531Tyr
ENST00000638240.1:c.513+2433C>T	ENSP00000492446.1:n.513+2433C>T
ENST00000313755.9:n.2357G>A (PRODH)
ENST00000334029.6:c.1268G>A (PRODH)	ENSP00000334726.2:p.Cys423Tyr
ENST00000357068.10:c.1592G>A (PRODH)	ENSP00000349577.6:p.Cys531Tyr
ENST00000420436.5:c.1268G>A (PRODH)	ENSP00000410805.1:p.Cys423Tyr
ENST00000429300.5:n.1963G>A (PRODH)
ENST00000482858.5:n.4072G>A (PRODH)
ENST00000483718.5:c.*2103C>T (DGCR6)	ENSP00000467483.1:n.*2103C>T
ENST00000491604.5:n.2501G>A (PRODH)
ENST00000610940.4:c.1592G>A (PRODH)	ENSP00000480347.1:p.Cys531Tyr
NM_001195226.1:c.1268G>A (PRODH)	NP_001182155.1:p.Cys423Tyr
NM_016335.4:c.1592G>A (PRODH)	NP_057419.4:p.Cys531Tyr
XM_011530278.1:c.1019G>A (PRODH)	XP_011528580.1:p.Cys340Tyr
XM_011530279.1:c.812G>A (PRODH)	XP_011528581.1:p.Cys271Tyr
XR_937876.1:n.1659G>A (PRODH)
NM_005675.5:c.*1772C>T (DGCR6)	NP_005666.2:n.*1772C>T
NM_001195226.2:c.1268G>A (PRODH)	NP_001182155.2:p.Cys423Tyr
NM_016335.5:c.1592G>A (PRODH)	NP_057419.5:p.Cys531Tyr
NM_016335.6:c.1592G>A (PRODH) MANE Select	NP_057419.5:p.Cys531Tyr