Canonical Allele Identifier: CA2395639486

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18936232G= , CM000684.2:g.18936232G=	GRCh38
NC_000022.10:g.18923745G= , CM000684.1:g.18923745G=	GRCh37
NC_000022.9:g.17303745G=	NCBI36
NG_008226.2:g.5322C=
NG_008226.3:g.5322C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016335.6:c.56C= MANE Select	NP_057419.5:p.Pro19=
ENST00000357068.11:c.56C= MANE Select	ENSP00000349577.6:p.Pro19=
NM_001195226.1:c.-52+158C=	NP_001182155.1:n.-52+158C=
NM_001195226.2:c.-52+158C=	NP_001182155.2:n.-52+158C=
NM_016335.4:c.56C=	NP_057419.4:p.Pro19=
NM_016335.5:c.56C=	NP_057419.5:p.Pro19=
ENST00000334029.6:c.-52+158C=	ENSP00000334726.2:n.-52+158C=
ENST00000357068.10:c.56C=	ENSP00000349577.6:p.Pro19=
ENST00000420436.5:c.-97C=	ENSP00000410805.1:n.-97C=
ENST00000457083.1:c.35C=
ENST00000491604.5:n.64C=
ENST00000610940.4:c.56C=	ENSP00000480347.1:p.Pro19=
ENST00000638240.1:c.514-3441G=	ENSP00000492446.1:n.514-3441G=
XM_011530278.1:c.-453C=	XP_011528580.1:n.-453C=
XR_937876.1:n.89C=