Canonical Allele Identifier: CA2395633526

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18913148T= , CM000684.2:g.18913148T= GRCh38
NC_000022.10:g.18900661T= , CM000684.1:g.18900661T= GRCh37
NC_000022.9:g.17280661T= NCBI36
NG_008226.2:g.28406A=
NG_009052.1:g.11926T=
NG_008226.3:g.28406A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357068.11:c.*27A= (PRODH) MANE Select ENSP00000349577.6:n.*27A=
ENST00000638240.1:c.513+2120T= ENSP00000492446.1:n.513+2120T=
ENST00000313755.9:n.2595A= (PRODH)
ENST00000334029.6:c.*27A= (PRODH) ENSP00000334726.2:n.*27A=
ENST00000357068.10:c.*27A= (PRODH) ENSP00000349577.6:n.*27A=
ENST00000420436.5:c.*27A= (PRODH) ENSP00000410805.1:n.*27A=
ENST00000429300.5:n.2201A= (PRODH)
ENST00000482858.5:n.4310A= (PRODH)
ENST00000483718.5:c.*1790T= (DGCR6) ENSP00000467483.1:n.*1790T=
ENST00000491604.5:n.2739A= (PRODH)
ENST00000610940.4:c.*27A= (PRODH) ENSP00000480347.1:n.*27A=
NM_001195226.1:c.*27A= (PRODH) NP_001182155.1:n.*27A=
NM_016335.4:c.*27A= (PRODH) NP_057419.4:n.*27A=
XM_011530278.1:c.*27A= (PRODH) XP_011528580.1:n.*27A=
XM_011530279.1:c.*27A= (PRODH) XP_011528581.1:n.*27A=
XR_937876.1:n.1897A= (PRODH)
NM_005675.5:c.*1459T= (DGCR6) NP_005666.2:n.*1459T=
NM_001195226.2:c.*27A= (PRODH) NP_001182155.2:n.*27A=
NM_016335.5:c.*27A= (PRODH) NP_057419.5:n.*27A=
NM_016335.6:c.*27A= (PRODH) MANE Select NP_057419.5:n.*27A=