Canonical Allele Identifier: CA16595738

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18914365C>G , CM000684.2:g.18914365C>G	GRCh38
NC_000022.10:g.18901878C>G , CM000684.1:g.18901878C>G	GRCh37
NC_000022.9:g.17281878C>G	NCBI36
NG_008226.2:g.27189G>C
NG_008226.3:g.27189G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_016335.6:c.1527-839G>C MANE Select	NP_057419.5:n.1527-839G>C
ENST00000357068.11:c.1527-839G>C MANE Select	ENSP00000349577.6:n.1527-839G>C
NM_001195226.1:c.1203-839G>C	NP_001182155.1:n.1203-839G>C
NM_001195226.2:c.1203-839G>C	NP_001182155.2:n.1203-839G>C
NM_016335.4:c.1527-839G>C	NP_057419.4:n.1527-839G>C
NM_016335.5:c.1527-839G>C	NP_057419.5:n.1527-839G>C
ENST00000313755.9:n.2292-839G>C
ENST00000334029.6:c.1203-839G>C	ENSP00000334726.2:n.1203-839G>C
ENST00000357068.10:c.1527-839G>C	ENSP00000349577.6:n.1527-839G>C
ENST00000420436.5:c.1203-839G>C	ENSP00000410805.1:n.1203-839G>C
ENST00000429300.5:n.1898-839G>C
ENST00000482858.5:n.4007-839G>C
ENST00000491604.5:n.2436-839G>C
ENST00000610940.4:c.1527-839G>C	ENSP00000480347.1:n.1527-839G>C
ENST00000638240.1:c.513+3337C>G	ENSP00000492446.1:n.513+3337C>G
XM_011530278.1:c.954-839G>C	XP_011528580.1:n.954-839G>C
XM_011530279.1:c.747-839G>C	XP_011528581.1:n.747-839G>C
XR_937876.1:n.1594-839G>C