Canonical Allele Identifier: CA9443709
Gene: PRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40394290_40394295del , CM000681.2:g.40394290_40394295del GRCh38
NC_000019.9:g.40900197_40900202del , CM000681.1:g.40900197_40900202del GRCh37
NC_000019.8:g.45592037_45592042del NCBI36
NG_007979.1:g.24087_24092del , LRG_265:g.24087_24092del
NG_051224.1:g.944_949del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324001.8:c.4074_4079del MANE Select ENSP00000326018.6:p.Glu1359_Glu1360del
ENST00000673881.1:c.3657_3662del ENSP00000501070.1:p.Glu1220_Glu1221del
ENST00000674005.2:c.4359_4364del ENSP00000501261.1:p.Glu1454_Glu1455del
ENST00000674773.1:c.3657_3662del ENSP00000502579.1:p.Glu1220_Glu1221del
ENST00000675517.1:c.3949_3954del
ENST00000676076.1:c.3935_3940del
ENST00000676260.1:c.4036_4041del
ENST00000676316.1:c.3961_3966del
ENST00000291825.11:c.*4279_*4284del ENSP00000291825.6:n.*4279_*4284del
ENST00000324001.7:c.4074_4079del ENSP00000326018.6:p.Glu1359_Glu1360del
NM_020956.2:c.*4279_*4284del , LRG_265t1:c.*4279_*4284del NP_066007.1:n.*4279_*4284del
NM_181882.2:c.4074_4079del , LRG_265t2:c.4074_4079del NP_870998.2:p.Glu1359_Glu1360del
XM_011527171.1:c.4074_4079del XP_011525473.1:p.Glu1359_Glu1360del
XM_011527171.2:c.4074_4079del XP_011525473.1:p.Glu1359_Glu1360del
XM_017027046.1:c.3972_3977del XP_016882535.1:p.Glu1325_Glu1326del
XM_017027047.1:c.3972_3977del XP_016882536.1:p.Glu1325_Glu1326del
NM_181882.3:c.4074_4079del MANE Select NP_870998.2:p.Glu1359_Glu1360del