Canonical Allele Identifier: CA638502671

Linked Data

dbSNP Id: rs1208973665

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913139_18913144dup , CM000684.2:g.18913139_18913144dup GRCh38
NC_000022.10:g.18900652_18900657dup , CM000684.1:g.18900652_18900657dup GRCh37
NC_000022.9:g.17280652_17280657dup NCBI36
NG_008226.2:g.28410_28415dup
NG_009052.1:g.11917_11922dup
NG_008226.3:g.28410_28415dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*31_*36dup (PRODH) MANE Select ENSP00000349577.6:n.*31_*36dup
ENST00000638240.1:c.513+2111_513+2116dup ENSP00000492446.1:n.513+2111_513+2116dup
ENST00000313755.9:n.2599_2604dup (PRODH)
ENST00000334029.6:c.*31_*36dup (PRODH) ENSP00000334726.2:n.*31_*36dup
ENST00000357068.10:c.*31_*36dup (PRODH) ENSP00000349577.6:n.*31_*36dup
ENST00000420436.5:c.*31_*36dup (PRODH) ENSP00000410805.1:n.*31_*36dup
ENST00000429300.5:n.2205_2210dup (PRODH)
ENST00000482858.5:n.4314_4319dup (PRODH)
ENST00000483718.5:c.*1781_*1786dup (DGCR6) ENSP00000467483.1:n.*1781_*1786dup
ENST00000491604.5:n.2743_2748dup (PRODH)
ENST00000610940.4:c.*31_*36dup (PRODH) ENSP00000480347.1:n.*31_*36dup
NM_001195226.1:c.*31_*36dup (PRODH) NP_001182155.1:n.*31_*36dup
NM_016335.4:c.*31_*36dup (PRODH) NP_057419.4:n.*31_*36dup
XM_011530278.1:c.*31_*36dup (PRODH) XP_011528580.1:n.*31_*36dup
XM_011530279.1:c.*31_*36dup (PRODH) XP_011528581.1:n.*31_*36dup
XR_937876.1:n.1901_1906dup (PRODH)
NM_005675.5:c.*1450_*1455dup (DGCR6) NP_005666.2:n.*1450_*1455dup
NM_001195226.2:c.*31_*36dup (PRODH) NP_001182155.2:n.*31_*36dup
NM_016335.5:c.*31_*36dup (PRODH) NP_057419.5:n.*31_*36dup
NM_016335.6:c.*31_*36dup (PRODH) MANE Select NP_057419.5:n.*31_*36dup