Canonical Allele Identifier: CA10094866

Gene: PRODH DGCR6

Linked Data

• dbSNP Id: rs368092146
• ExAC: 22:18900901 G / T
• gnomAD v2: 22-18900901-G-T
• MyVariant Identifiers: chr22:g.18900901G>T (hg19) ; chr22:g.18913388G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913388G>T , CM000684.2:g.18913388G>T	GRCh38
NC_000022.10:g.18900901G>T , CM000684.1:g.18900901G>T	GRCh37
NC_000022.9:g.17280901G>T	NCBI36
NG_008226.2:g.28166C>A
NG_009052.1:g.12166G>T
NG_008226.3:g.28166C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1616-26C>A (PRODH) MANE Select	ENSP00000349577.6:n.1616-26C>A
ENST00000638240.1:c.513+2360G>T	ENSP00000492446.1:n.513+2360G>T
ENST00000313755.9:n.2381-26C>A (PRODH)
ENST00000334029.6:c.1292-26C>A (PRODH)	ENSP00000334726.2:n.1292-26C>A
ENST00000357068.10:c.1616-26C>A (PRODH)	ENSP00000349577.6:n.1616-26C>A
ENST00000420436.5:c.1292-26C>A (PRODH)	ENSP00000410805.1:n.1292-26C>A
ENST00000429300.5:n.1987-26C>A (PRODH)
ENST00000482858.5:n.4096-26C>A (PRODH)
ENST00000483718.5:c.*2030G>T (DGCR6)	ENSP00000467483.1:n.*2030G>T
ENST00000491604.5:n.2525-26C>A (PRODH)
ENST00000610940.4:c.1616-26C>A (PRODH)	ENSP00000480347.1:n.1616-26C>A
NM_001195226.1:c.1292-26C>A (PRODH)	NP_001182155.1:n.1292-26C>A
NM_016335.4:c.1616-26C>A (PRODH)	NP_057419.4:n.1616-26C>A
XM_011530278.1:c.1043-26C>A (PRODH)	XP_011528580.1:n.1043-26C>A
XM_011530279.1:c.836-26C>A (PRODH)	XP_011528581.1:n.836-26C>A
XR_937876.1:n.1683-26C>A (PRODH)
NM_005675.5:c.*1699G>T (DGCR6)	NP_005666.2:n.*1699G>T
NM_001195226.2:c.1292-26C>A (PRODH)	NP_001182155.2:n.1292-26C>A
NM_016335.5:c.1616-26C>A (PRODH)	NP_057419.5:n.1616-26C>A
NM_016335.6:c.1616-26C>A (PRODH) MANE Select	NP_057419.5:n.1616-26C>A