Canonical Allele Identifier: CA9443710
Gene: PRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40394293_40394295dup , CM000681.2:g.40394293_40394295dup GRCh38
NC_000019.9:g.40900200_40900202dup , CM000681.1:g.40900200_40900202dup GRCh37
NC_000019.8:g.45592040_45592042dup NCBI36
NG_007979.1:g.24090_24092dup , LRG_265:g.24090_24092dup
NG_051224.1:g.947_949dup

Transcript Alleles

HGVS Amino-acid Change
NM_181882.3:c.4077_4079dup MANE Select NP_870998.2:p.Glu1360_Glu1361insGlu
ENST00000324001.8:c.4077_4079dup MANE Select ENSP00000326018.6:p.Glu1360_Glu1361insGlu
NM_020956.2:c.*4282_*4284dup , LRG_265t1:c.*4282_*4284dup NP_066007.1:n.*4282_*4284dup
NM_181882.2:c.4077_4079dup , LRG_265t2:c.4077_4079dup NP_870998.2:p.Glu1360_Glu1361insGlu
ENST00000291825.11:c.*4282_*4284dup ENSP00000291825.6:n.*4282_*4284dup
ENST00000324001.7:c.4077_4079dup ENSP00000326018.6:p.Glu1360_Glu1361insGlu
ENST00000673881.1:c.3660_3662dup ENSP00000501070.1:p.Glu1221_Glu1222insGlu
ENST00000674005.2:c.4362_4364dup ENSP00000501261.1:p.Glu1455_Glu1456insGlu
ENST00000674773.1:c.3660_3662dup ENSP00000502579.1:p.Glu1221_Glu1222insGlu
ENST00000675517.1:c.3952_3954dup
ENST00000676076.1:c.3938_3940dup
ENST00000676260.1:c.4039_4041dup
ENST00000676316.1:c.3964_3966dup
XM_011527171.1:c.4077_4079dup XP_011525473.1:p.Glu1360_Glu1361insGlu
XM_011527171.2:c.4077_4079dup XP_011525473.1:p.Glu1360_Glu1361insGlu
XM_017027046.1:c.3975_3977dup XP_016882535.1:p.Glu1326_Glu1327insGlu
XM_017027047.1:c.3975_3977dup XP_016882536.1:p.Glu1326_Glu1327insGlu