Canonical Allele Identifier: CA2655228902

Gene: PRODH DGCR6

Linked Data

• gnomAD v4: 22-18913155-TAAGGGTGTGCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18913156_18913167del , CM000684.2:g.18913156_18913167del	GRCh38
NC_000022.10:g.18900669_18900680del , CM000684.1:g.18900669_18900680del	GRCh37
NC_000022.9:g.17280669_17280680del	NCBI36
NG_008226.2:g.28387_28398del
NG_009052.1:g.11934_11945del
NG_008226.3:g.28387_28398del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.*8_*19del (PRODH) MANE Select	ENSP00000349577.6:n.*8_*19del
ENST00000638240.1:c.513+2128_513+2139del	ENSP00000492446.1:n.513+2128_513+2139del
ENST00000313755.9:n.2576_2587del (PRODH)
ENST00000334029.6:c.*8_*19del (PRODH)	ENSP00000334726.2:n.*8_*19del
ENST00000357068.10:c.*8_*19del (PRODH)	ENSP00000349577.6:n.*8_*19del
ENST00000420436.5:c.*8_*19del (PRODH)	ENSP00000410805.1:n.*8_*19del
ENST00000429300.5:n.2182_2193del (PRODH)
ENST00000482858.5:n.4291_4302del (PRODH)
ENST00000483718.5:c.*1798_*1809del (DGCR6)	ENSP00000467483.1:n.*1798_*1809del
ENST00000491604.5:n.2720_2731del (PRODH)
ENST00000610940.4:c.*8_*19del (PRODH)	ENSP00000480347.1:n.*8_*19del
NM_001195226.1:c.*8_*19del (PRODH)	NP_001182155.1:n.*8_*19del
NM_016335.4:c.*8_*19del (PRODH)	NP_057419.4:n.*8_*19del
XM_011530278.1:c.*8_*19del (PRODH)	XP_011528580.1:n.*8_*19del
XM_011530279.1:c.*8_*19del (PRODH)	XP_011528581.1:n.*8_*19del
XR_937876.1:n.1878_1889del (PRODH)
NM_005675.5:c.*1467_*1478del (DGCR6)	NP_005666.2:n.*1467_*1478del
NM_001195226.2:c.*8_*19del (PRODH)	NP_001182155.2:n.*8_*19del
NM_016335.5:c.*8_*19del (PRODH)	NP_057419.5:n.*8_*19del
NM_016335.6:c.*8_*19del (PRODH) MANE Select	NP_057419.5:n.*8_*19del