Canonical Allele Identifier: CA10095172

Gene: PRODH

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18921424C>G , CM000684.2:g.18921424C>G	GRCh38
NC_000022.10:g.18908937C>G , CM000684.1:g.18908937C>G	GRCh37
NC_000022.9:g.17288937C>G	NCBI36
NG_008226.2:g.20130G>C
NG_008226.3:g.20130G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.930-1G>C MANE Select	ENSP00000349577.6:n.930-1G>C
ENST00000638240.1:c.513+10396C>G	ENSP00000492446.1:n.513+10396C>G
ENST00000313755.9:n.151G>C
ENST00000334029.6:c.606-1G>C	ENSP00000334726.2:n.606-1G>C
ENST00000357068.10:c.930-1G>C	ENSP00000349577.6:n.930-1G>C
ENST00000420436.5:c.606-1G>C	ENSP00000410805.1:n.606-1G>C
ENST00000429300.5:n.1267-1G>C
ENST00000438924.5:c.511-1G>C
ENST00000446371.1:n.116G>C
ENST00000482858.5:n.1866G>C
ENST00000491604.5:n.1838G>C
ENST00000609229.1:n.131G>C
ENST00000610940.4:c.930-1G>C	ENSP00000480347.1:n.930-1G>C
NM_001195226.1:c.606-1G>C	NP_001182155.1:n.606-1G>C
NM_016335.4:c.930-1G>C	NP_057419.4:n.930-1G>C
XM_011530278.1:c.357-1G>C	XP_011528580.1:n.357-1G>C
XM_011530279.1:c.150-1G>C	XP_011528581.1:n.150-1G>C
XR_937876.1:n.963-1G>C
NM_001195226.2:c.606-1G>C	NP_001182155.2:n.606-1G>C
NM_016335.5:c.930-1G>C	NP_057419.5:n.930-1G>C
NM_016335.6:c.930-1G>C MANE Select	NP_057419.5:n.930-1G>C