Canonical Allele Identifier: CA2395636062

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18922389A= , CM000684.2:g.18922389A=	GRCh38
NC_000022.10:g.18909902A= , CM000684.1:g.18909902A=	GRCh37
NC_000022.9:g.17289902A=	NCBI36
NG_008226.2:g.19165T=
NG_008226.3:g.19165T=

Transcript Alleles

HGVS	Amino-acid Change
NM_016335.6:c.865T= MANE Select	NP_057419.5:p.Leu289=
ENST00000357068.11:c.865T= MANE Select	ENSP00000349577.6:p.Leu289=
NM_001195226.1:c.541T=	NP_001182155.1:p.Leu181=
NM_001195226.2:c.541T=	NP_001182155.2:p.Leu181=
NM_016335.4:c.865T=	NP_057419.4:p.Leu289=
NM_016335.5:c.865T=	NP_057419.5:p.Leu289=
ENST00000334029.6:c.541T=	ENSP00000334726.2:p.Leu181=
ENST00000357068.10:c.865T=	ENSP00000349577.6:p.Leu289=
ENST00000399694.1:n.329T=
ENST00000420436.5:c.541T=	ENSP00000410805.1:p.Leu181=
ENST00000429300.5:n.1202T=
ENST00000438924.5:c.446T=
ENST00000450579.1:c.388T=	ENSP00000396806.1:p.Leu130=
ENST00000482858.5:n.901T=
ENST00000491604.5:n.873T=
ENST00000610940.4:c.865T=	ENSP00000480347.1:p.Leu289=
ENST00000638240.1:c.513+11361A=	ENSP00000492446.1:n.513+11361A=
XM_011530278.1:c.292T=	XP_011528580.1:p.Leu98=
XM_011530279.1:c.85T=	XP_011528581.1:p.Leu29=
XR_937876.1:n.898T=