Canonical Allele Identifier: CA512940990

Gene: PRODH

Linked Data

• dbSNP Id: rs527793360
• MyVariant Identifiers: chr22:g.18905897A>C (hg19) ; chr22:g.18918384A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18918384A>C , CM000684.2:g.18918384A>C	GRCh38
NC_000022.10:g.18905897A>C , CM000684.1:g.18905897A>C	GRCh37
NC_000022.9:g.17285897A>C	NCBI36
NG_008226.2:g.23170T>G
NG_008226.3:g.23170T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000357068.11:c.1359T>G MANE Select	ENSP00000349577.6:p.Arg453=
ENST00000638240.1:c.513+7356A>C	ENSP00000492446.1:n.513+7356A>C
ENST00000313755.9:n.2124T>G
ENST00000334029.6:c.1035T>G	ENSP00000334726.2:p.Arg345=
ENST00000357068.10:c.1359T>G	ENSP00000349577.6:p.Arg453=
ENST00000420436.5:c.1035T>G	ENSP00000410805.1:p.Arg345=
ENST00000429300.5:n.1730T>G
ENST00000482858.5:n.3839T>G
ENST00000491604.5:n.2268T>G
ENST00000609229.1:n.2212T>G
ENST00000610940.4:c.1359T>G	ENSP00000480347.1:p.Arg453=
NM_001195226.1:c.1035T>G	NP_001182155.1:p.Arg345=
NM_016335.4:c.1359T>G	NP_057419.4:p.Arg453=
XM_011530278.1:c.786T>G	XP_011528580.1:p.Arg262=
XM_011530279.1:c.579T>G	XP_011528581.1:p.Arg193=
XR_937876.1:n.1426T>G
NM_001195226.2:c.1035T>G	NP_001182155.2:p.Arg345=
NM_016335.5:c.1359T>G	NP_057419.5:p.Arg453=
NM_016335.6:c.1359T>G MANE Select	NP_057419.5:p.Arg453=