Canonical Allele Identifier: CA2395633708

Gene: PRODH DGCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913537G= , CM000684.2:g.18913537G=	GRCh38
NC_000022.10:g.18901050G= , CM000684.1:g.18901050G=	GRCh37
NC_000022.9:g.17281050G=	NCBI36
NG_008226.2:g.28017C=
NG_009052.1:g.12315G=
NG_008226.3:g.28017C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1527-11C= (PRODH) MANE Select	ENSP00000349577.6:n.1527-11C=
ENST00000638240.1:c.513+2509G=	ENSP00000492446.1:n.513+2509G=
ENST00000313755.9:n.2292-11C= (PRODH)
ENST00000334029.6:c.1203-11C= (PRODH)	ENSP00000334726.2:n.1203-11C=
ENST00000357068.10:c.1527-11C= (PRODH)	ENSP00000349577.6:n.1527-11C=
ENST00000420436.5:c.1203-11C= (PRODH)	ENSP00000410805.1:n.1203-11C=
ENST00000429300.5:n.1898-11C= (PRODH)
ENST00000482858.5:n.4007-11C= (PRODH)
ENST00000483718.5:c.*2179G= (DGCR6)	ENSP00000467483.1:n.*2179G=
ENST00000491604.5:n.2436-11C= (PRODH)
ENST00000610940.4:c.1527-11C= (PRODH)	ENSP00000480347.1:n.1527-11C=
NM_001195226.1:c.1203-11C= (PRODH)	NP_001182155.1:n.1203-11C=
NM_016335.4:c.1527-11C= (PRODH)	NP_057419.4:n.1527-11C=
XM_011530278.1:c.954-11C= (PRODH)	XP_011528580.1:n.954-11C=
XM_011530279.1:c.747-11C= (PRODH)	XP_011528581.1:n.747-11C=
XR_937876.1:n.1594-11C= (PRODH)
NM_005675.5:c.*1848G= (DGCR6)	NP_005666.2:n.*1848G=
NM_001195226.2:c.1203-11C= (PRODH)	NP_001182155.2:n.1203-11C=
NM_016335.5:c.1527-11C= (PRODH)	NP_057419.5:n.1527-11C=
NM_016335.6:c.1527-11C= (PRODH) MANE Select	NP_057419.5:n.1527-11C=