Canonical Allele Identifier: CA410639143

Gene: PRODH DGCR6

Linked Data

• MyVariant Identifiers: chr22:g.18901017G>T (hg19) ; chr22:g.18913504G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913504G>T , CM000684.2:g.18913504G>T	GRCh38
NC_000022.10:g.18901017G>T , CM000684.1:g.18901017G>T	GRCh37
NC_000022.9:g.17281017G>T	NCBI36
NG_008226.2:g.28050C>A
NG_009052.1:g.12282G>T
NG_008226.3:g.28050C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1549C>A (PRODH) MANE Select	ENSP00000349577.6:p.Pro517Thr
ENST00000638240.1:c.513+2476G>T	ENSP00000492446.1:n.513+2476G>T
ENST00000313755.9:n.2314C>A (PRODH)
ENST00000334029.6:c.1225C>A (PRODH)	ENSP00000334726.2:p.Pro409Thr
ENST00000357068.10:c.1549C>A (PRODH)	ENSP00000349577.6:p.Pro517Thr
ENST00000420436.5:c.1225C>A (PRODH)	ENSP00000410805.1:p.Pro409Thr
ENST00000429300.5:n.1920C>A (PRODH)
ENST00000482858.5:n.4029C>A (PRODH)
ENST00000483718.5:c.*2146G>T (DGCR6)	ENSP00000467483.1:n.*2146G>T
ENST00000491604.5:n.2458C>A (PRODH)
ENST00000610940.4:c.1549C>A (PRODH)	ENSP00000480347.1:p.Pro517Thr
NM_001195226.1:c.1225C>A (PRODH)	NP_001182155.1:p.Pro409Thr
NM_016335.4:c.1549C>A (PRODH)	NP_057419.4:p.Pro517Thr
XM_011530278.1:c.976C>A (PRODH)	XP_011528580.1:p.Pro326Thr
XM_011530279.1:c.769C>A (PRODH)	XP_011528581.1:p.Pro257Thr
XR_937876.1:n.1616C>A (PRODH)
NM_005675.5:c.*1815G>T (DGCR6)	NP_005666.2:n.*1815G>T
NM_001195226.2:c.1225C>A (PRODH)	NP_001182155.2:p.Pro409Thr
NM_016335.5:c.1549C>A (PRODH)	NP_057419.5:p.Pro517Thr
NM_016335.6:c.1549C>A (PRODH) MANE Select	NP_057419.5:p.Pro517Thr