Canonical Allele Identifier: CA10094886

Gene: PRODH DGCR6

Linked Data

• dbSNP Id: rs193919334
• ExAC: 22:18901005 G / T
• gnomAD v4: 22-18913492-G-T
• MyVariant Identifiers: chr22:g.18901005G>T (hg19) ; chr22:g.18913492G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913492G>T , CM000684.2:g.18913492G>T	GRCh38
NC_000022.10:g.18901005G>T , CM000684.1:g.18901005G>T	GRCh37
NC_000022.9:g.17281005G>T	NCBI36
NG_008226.2:g.28062C>A
NG_009052.1:g.12270G>T
NG_008226.3:g.28062C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357068.11:c.1561C>A (PRODH) MANE Select	ENSP00000349577.6:p.Arg521=
ENST00000638240.1:c.513+2464G>T	ENSP00000492446.1:n.513+2464G>T
ENST00000313755.9:n.2326C>A (PRODH)
ENST00000334029.6:c.1237C>A (PRODH)	ENSP00000334726.2:p.Arg413=
ENST00000357068.10:c.1561C>A (PRODH)	ENSP00000349577.6:p.Arg521=
ENST00000420436.5:c.1237C>A (PRODH)	ENSP00000410805.1:p.Arg413=
ENST00000429300.5:n.1932C>A (PRODH)
ENST00000482858.5:n.4041C>A (PRODH)
ENST00000483718.5:c.*2134G>T (DGCR6)	ENSP00000467483.1:n.*2134G>T
ENST00000491604.5:n.2470C>A (PRODH)
ENST00000610940.4:c.1561C>A (PRODH)	ENSP00000480347.1:p.Arg521=
NM_001195226.1:c.1237C>A (PRODH)	NP_001182155.1:p.Gln413Lys
NM_016335.4:c.1561C>A (PRODH)	NP_057419.4:p.Gln521Lys
XM_011530278.1:c.988C>A (PRODH)	XP_011528580.1:p.Arg330=
XM_011530279.1:c.781C>A (PRODH)	XP_011528581.1:p.Arg261=
XR_937876.1:n.1628C>A (PRODH)
NM_005675.5:c.*1803G>T (DGCR6)	NP_005666.2:n.*1803G>T
NM_001195226.2:c.1237C>A (PRODH)	NP_001182155.2:p.Arg413=
NM_016335.5:c.1561C>A (PRODH)	NP_057419.5:p.Arg521=
NM_016335.6:c.1561C>A (PRODH) MANE Select	NP_057419.5:p.Arg521=