Canonical Allele Identifier: CA410649398

Gene: PRODH

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18925176T>A , CM000684.2:g.18925176T>A	GRCh38
NC_000022.10:g.18912689T>A , CM000684.1:g.18912689T>A	GRCh37
NC_000022.9:g.17292689T>A	NCBI36
NG_008226.2:g.16378A>T
NG_008226.3:g.16378A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357068.11:c.542A>T MANE Select	ENSP00000349577.6:p.Tyr181Phe
ENST00000638240.1:c.513+14148T>A	ENSP00000492446.1:n.513+14148T>A
ENST00000334029.6:c.218A>T	ENSP00000334726.2:p.Tyr73Phe
ENST00000357068.10:c.542A>T	ENSP00000349577.6:p.Tyr181Phe
ENST00000420436.5:c.218A>T	ENSP00000410805.1:p.Tyr73Phe
ENST00000438924.5:c.188A>T
ENST00000450579.1:c.65A>T	ENSP00000396806.1:p.Tyr22Phe
ENST00000457083.1:c.312A>T
ENST00000482858.5:n.397A>T
ENST00000491604.5:n.550A>T
ENST00000496625.1:n.181A>T
ENST00000610940.4:c.542A>T	ENSP00000480347.1:p.Tyr181Phe
NM_001195226.1:c.218A>T	NP_001182155.1:p.Tyr73Phe
NM_016335.4:c.542A>T	NP_057419.4:p.Tyr181Phe
XM_011530278.1:c.34A>T	XP_011528580.1:p.Thr12Ser
XR_937876.1:n.575A>T
NM_001195226.2:c.218A>T	NP_001182155.2:p.Tyr73Phe
NM_016335.5:c.542A>T	NP_057419.5:p.Tyr181Phe
NM_016335.6:c.542A>T MANE Select	NP_057419.5:p.Tyr181Phe