Canonical Allele Identifier: CA2395635038

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18918421A= , CM000684.2:g.18918421A=	GRCh38
NC_000022.10:g.18905934A= , CM000684.1:g.18905934A=	GRCh37
NC_000022.9:g.17285934A=	NCBI36
NG_008226.2:g.23133T=
NG_008226.3:g.23133T=

Transcript Alleles

HGVS	Amino-acid Change
NM_016335.6:c.1322T= MANE Select	NP_057419.5:p.Leu441=
ENST00000357068.11:c.1322T= MANE Select	ENSP00000349577.6:p.Leu441=
NM_001195226.1:c.998T=	NP_001182155.1:p.Leu333=
NM_001195226.2:c.998T=	NP_001182155.2:p.Leu333=
NM_016335.4:c.1322T=	NP_057419.4:p.Leu441=
NM_016335.5:c.1322T=	NP_057419.5:p.Leu441=
ENST00000313755.9:n.2087T=
ENST00000334029.6:c.998T=	ENSP00000334726.2:p.Leu333=
ENST00000357068.10:c.1322T=	ENSP00000349577.6:p.Leu441=
ENST00000420436.5:c.998T=	ENSP00000410805.1:p.Leu333=
ENST00000429300.5:n.1693T=
ENST00000482858.5:n.3802T=
ENST00000491604.5:n.2231T=
ENST00000609229.1:n.2175T=
ENST00000610940.4:c.1322T=	ENSP00000480347.1:p.Leu441=
ENST00000638240.1:c.513+7393A=	ENSP00000492446.1:n.513+7393A=
XM_011530278.1:c.749T=	XP_011528580.1:p.Leu250=
XM_011530279.1:c.542T=	XP_011528581.1:p.Leu181=
XR_937876.1:n.1389T=