Canonical Allele Identifier: CA2818372165

Gene: PRODH DGCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913086A>C , CM000684.2:g.18913086A>C	GRCh38
NC_000022.10:g.18900599A>C , CM000684.1:g.18900599A>C	GRCh37
NC_000022.9:g.17280599A>C	NCBI36
NG_008226.2:g.28468T>G
NG_009052.1:g.11864A>C
NG_008226.3:g.28468T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.*89T>G (PRODH) MANE Select	ENSP00000349577.6:n.*89T>G
ENST00000638240.1:c.513+2058A>C	ENSP00000492446.1:n.513+2058A>C
ENST00000313755.9:n.2657T>G (PRODH)
ENST00000334029.6:c.*89T>G (PRODH)	ENSP00000334726.2:n.*89T>G
ENST00000357068.10:c.*89T>G (PRODH)	ENSP00000349577.6:n.*89T>G
ENST00000420436.5:c.*89T>G (PRODH)	ENSP00000410805.1:n.*89T>G
ENST00000429300.5:n.2263T>G (PRODH)
ENST00000482858.5:n.4372T>G (PRODH)
ENST00000483718.5:c.*1728A>C (DGCR6)	ENSP00000467483.1:n.*1728A>C
ENST00000491604.5:n.2801T>G (PRODH)
ENST00000610940.4:c.*89T>G (PRODH)	ENSP00000480347.1:n.*89T>G
NM_001195226.1:c.*89T>G (PRODH)	NP_001182155.1:n.*89T>G
NM_016335.4:c.*89T>G (PRODH)	NP_057419.4:n.*89T>G
XM_011530278.1:c.*89T>G (PRODH)	XP_011528580.1:n.*89T>G
XM_011530279.1:c.*89T>G (PRODH)	XP_011528581.1:n.*89T>G
XR_937876.1:n.1959T>G (PRODH)
NM_005675.5:c.*1397A>C (DGCR6)	NP_005666.2:n.*1397A>C
NM_001195226.2:c.*89T>G (PRODH)	NP_001182155.2:n.*89T>G
NM_016335.5:c.*89T>G (PRODH)	NP_057419.5:n.*89T>G
NM_016335.6:c.*89T>G (PRODH) MANE Select	NP_057419.5:n.*89T>G