Canonical Allele Identifier: CA2335961583
Gene: PRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40396331_40396332delinsGC , CM000681.2:g.40396331_40396332delinsGC GRCh38
NC_000019.9:g.40902238_40902239delinsGC , CM000681.1:g.40902238_40902239delinsGC GRCh37
NC_000019.8:g.45594078_45594079delinsGC NCBI36
NG_007979.1:g.22033_22034delinsGC , LRG_265:g.22033_22034delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000324001.8:c.2020_2021delinsGC MANE Select ENSP00000326018.6:p.Ala674=
ENST00000673881.1:c.1603_1604delinsGC ENSP00000501070.1:p.Ala535=
ENST00000674005.2:c.2305_2306delinsGC ENSP00000501261.1:p.Ala769=
ENST00000674773.1:c.1603_1604delinsGC ENSP00000502579.1:p.Ala535=
ENST00000675517.1:c.1895_1896delinsGC
ENST00000676076.1:c.1881_1882delinsGC
ENST00000676260.1:c.1982_1983delinsGC
ENST00000676316.1:c.1907_1908delinsGC
ENST00000291825.11:c.*2225_*2226delinsGC ENSP00000291825.6:n.*2225_*2226delinsGC
ENST00000324001.7:c.2020_2021delinsGC ENSP00000326018.6:p.Ala674=
NM_020956.2:c.*2225_*2226delinsGC , LRG_265t1:c.*2225_*2226delinsGC NP_066007.1:n.*2225_*2226delinsGC
NM_181882.2:c.2020_2021delinsGC , LRG_265t2:c.2020_2021delinsGC NP_870998.2:p.Ala674=
XM_011527171.1:c.2020_2021delinsGC XP_011525473.1:p.Ala674=
XM_011527171.2:c.2020_2021delinsGC XP_011525473.1:p.Ala674=
XM_017027046.1:c.1918_1919delinsGC XP_016882535.1:p.Ala640=
XM_017027047.1:c.1918_1919delinsGC XP_016882536.1:p.Ala640=
NM_181882.3:c.2020_2021delinsGC MANE Select NP_870998.2:p.Ala674=