Canonical Allele Identifier: CA1139666956

Gene: PRODH

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18918380_18918381delinsAT , CM000684.2:g.18918380_18918381delinsAT	GRCh38
NC_000022.10:g.18905893_18905894delinsAT , CM000684.1:g.18905893_18905894delinsAT	GRCh37
NC_000022.9:g.17285893_17285894delinsAT	NCBI36
NG_008226.2:g.23173_23174delinsAT
NG_008226.3:g.23173_23174delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.1362_1363delinsAT MANE Select	ENSP00000349577.6:p.Ala455Ser
ENST00000638240.1:c.513+7352_513+7353delinsAT	ENSP00000492446.1:n.513+7352_513+7353delinsAT
ENST00000313755.9:n.2127_2128delinsAT
ENST00000334029.6:c.1038_1039delinsAT	ENSP00000334726.2:p.Ala347Ser
ENST00000357068.10:c.1362_1363delinsAT	ENSP00000349577.6:p.Ala455Ser
ENST00000420436.5:c.1038_1039delinsAT	ENSP00000410805.1:p.Ala347Ser
ENST00000429300.5:n.1733_1734delinsAT
ENST00000482858.5:n.3842_3843delinsAT
ENST00000491604.5:n.2271_2272delinsAT
ENST00000609229.1:n.2215_2216delinsAT
ENST00000610940.4:c.1362_1363delinsAT	ENSP00000480347.1:p.Ala455Ser
NM_001195226.1:c.1038_1039delinsAT	NP_001182155.1:p.Ala347Ser
NM_016335.4:c.1362_1363delinsAT	NP_057419.4:p.Ala455Ser
XM_011530278.1:c.789_790delinsAT	XP_011528580.1:p.Ala264Ser
XM_011530279.1:c.582_583delinsAT	XP_011528581.1:p.Ala195Ser
XR_937876.1:n.1429_1430delinsAT
NM_001195226.2:c.1038_1039delinsAT	NP_001182155.2:p.Ala347Ser
NM_016335.5:c.1362_1363delinsAT	NP_057419.5:p.Ala455Ser
NM_016335.6:c.1362_1363delinsAT MANE Select	NP_057419.5:p.Ala455Ser