Canonical Allele Identifier: CA2395633520

Gene: PRODH DGCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913142_18913169delinsGGGTGCTGGAGGCTAAGGGTGTGCTGGC , CM000684.2:g.18913142_18913169delinsGGGTGCTGGAGGCTAAGGGTGTGCTGGC	GRCh38
NC_000022.10:g.18900655_18900682delinsGGGTGCTGGAGGCTAAGGGTGTGCTGGC , CM000684.1:g.18900655_18900682delinsGGGTGCTGGAGGCTAAGGGTGTGCTGGC	GRCh37
NC_000022.9:g.17280655_17280682delinsGGGTGCTGGAGGCTAAGGGTGTGCTGGC	NCBI36
NG_008226.2:g.28385_28412delinsGCCAGCACACCCTTAGCCTCCAGCACCC
NG_009052.1:g.11920_11947delinsGGGTGCTGGAGGCTAAGGGTGTGCTGGC
NG_008226.3:g.28385_28412delinsGCCAGCACACCCTTAGCCTCCAGCACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH) MANE Select	ENSP00000349577.6:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
ENST00000638240.1:c.513+2114_513+2141delinsGGGTGCTGGAGGCTAAGGGTGTGCTGGC	ENSP00000492446.1:n.513+2114_513+2141delinsGGGTGCTGGAGGCTAAGG...
ENST00000313755.9:n.2574_2601delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)
ENST00000334029.6:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)	ENSP00000334726.2:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
ENST00000357068.10:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)	ENSP00000349577.6:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
ENST00000420436.5:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)	ENSP00000410805.1:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
ENST00000429300.5:n.2180_2207delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)
ENST00000482858.5:n.4289_4316delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)
ENST00000483718.5:c.*1784_*1811delinsGGGTGCTGGAGGCTAAGGGTGTGCTGGC (DGCR6)	ENSP00000467483.1:n.*1784_*1811delinsGGGTGCTGGAGGCTAAGGGTGTGC...
ENST00000491604.5:n.2718_2745delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)
ENST00000610940.4:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)	ENSP00000480347.1:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
NM_001195226.1:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)	NP_001182155.1:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
NM_016335.4:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)	NP_057419.4:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
XM_011530278.1:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)	XP_011528580.1:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
XM_011530279.1:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)	XP_011528581.1:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
XR_937876.1:n.1876_1903delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)
NM_005675.5:c.*1453_*1480delinsGGGTGCTGGAGGCTAAGGGTGTGCTGGC (DGCR6)	NP_005666.2:n.*1453_*1480delinsGGGTGCTGGAGGCTAAGGGTGTGCTGGC
NM_001195226.2:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)	NP_001182155.2:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
NM_016335.5:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH)	NP_057419.5:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC
NM_016335.6:c.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC (PRODH) MANE Select	NP_057419.5:n.*6_*33delinsGCCAGCACACCCTTAGCCTCCAGCACCC