Canonical Allele Identifier: CA410649395

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18925175G>C , CM000684.2:g.18925175G>C	GRCh38
NC_000022.10:g.18912688G>C , CM000684.1:g.18912688G>C	GRCh37
NC_000022.9:g.17292688G>C	NCBI36
NG_008226.2:g.16379C>G
NG_008226.3:g.16379C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.543C>G MANE Select	ENSP00000349577.6:p.Tyr181Ter
ENST00000638240.1:c.513+14147G>C	ENSP00000492446.1:n.513+14147G>C
ENST00000334029.6:c.219C>G	ENSP00000334726.2:p.Tyr73Ter
ENST00000357068.10:c.543C>G	ENSP00000349577.6:p.Tyr181Ter
ENST00000420436.5:c.219C>G	ENSP00000410805.1:p.Tyr73Ter
ENST00000438924.5:c.189C>G
ENST00000450579.1:c.66C>G	ENSP00000396806.1:p.Tyr22Ter
ENST00000457083.1:c.313C>G
ENST00000482858.5:n.398C>G
ENST00000491604.5:n.551C>G
ENST00000496625.1:n.182C>G
ENST00000610940.4:c.543C>G	ENSP00000480347.1:p.Tyr181Ter
NM_001195226.1:c.219C>G	NP_001182155.1:p.Tyr73Ter
NM_016335.4:c.543C>G	NP_057419.4:p.Tyr181Ter
XM_011530278.1:c.35C>G	XP_011528580.1:p.Thr12Ser
XR_937876.1:n.576C>G
NM_001195226.2:c.219C>G	NP_001182155.2:p.Tyr73Ter
NM_016335.5:c.543C>G	NP_057419.5:p.Tyr181Ter
NM_016335.6:c.543C>G MANE Select	NP_057419.5:p.Tyr181Ter