Canonical Allele Identifier: CA2395633523

Gene: PRODH DGCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913145T= , CM000684.2:g.18913145T=	GRCh38
NC_000022.10:g.18900658T= , CM000684.1:g.18900658T=	GRCh37
NC_000022.9:g.17280658T=	NCBI36
NG_008226.2:g.28409A=
NG_009052.1:g.11923T=
NG_008226.3:g.28409A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.*30A= (PRODH) MANE Select	ENSP00000349577.6:n.*30A=
ENST00000638240.1:c.513+2117T=	ENSP00000492446.1:n.513+2117T=
ENST00000313755.9:n.2598A= (PRODH)
ENST00000334029.6:c.*30A= (PRODH)	ENSP00000334726.2:n.*30A=
ENST00000357068.10:c.*30A= (PRODH)	ENSP00000349577.6:n.*30A=
ENST00000420436.5:c.*30A= (PRODH)	ENSP00000410805.1:n.*30A=
ENST00000429300.5:n.2204A= (PRODH)
ENST00000482858.5:n.4313A= (PRODH)
ENST00000483718.5:c.*1787T= (DGCR6)	ENSP00000467483.1:n.*1787T=
ENST00000491604.5:n.2742A= (PRODH)
ENST00000610940.4:c.*30A= (PRODH)	ENSP00000480347.1:n.*30A=
NM_001195226.1:c.*30A= (PRODH)	NP_001182155.1:n.*30A=
NM_016335.4:c.*30A= (PRODH)	NP_057419.4:n.*30A=
XM_011530278.1:c.*30A= (PRODH)	XP_011528580.1:n.*30A=
XM_011530279.1:c.*30A= (PRODH)	XP_011528581.1:n.*30A=
XR_937876.1:n.1900A= (PRODH)
NM_005675.5:c.*1456T= (DGCR6)	NP_005666.2:n.*1456T=
NM_001195226.2:c.*30A= (PRODH)	NP_001182155.2:n.*30A=
NM_016335.5:c.*30A= (PRODH)	NP_057419.5:n.*30A=
NM_016335.6:c.*30A= (PRODH) MANE Select	NP_057419.5:n.*30A=