Canonical Allele Identifier: CA2841146540
Gene: PRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40395024dup , CM000681.2:g.40395024dup GRCh38
NC_000019.9:g.40900931dup , CM000681.1:g.40900931dup GRCh37
NC_000019.8:g.45592771dup NCBI36
NG_007979.1:g.23343dup , LRG_265:g.23343dup
NG_051224.1:g.200dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000324001.8:c.3330dup MANE Select ENSP00000326018.6:p.Arg1111GlufsTer27
ENST00000673881.1:c.2913dup ENSP00000501070.1:p.Arg972GlufsTer27
ENST00000674005.2:c.3615dup ENSP00000501261.1:p.Arg1206GlufsTer27
ENST00000674773.1:c.2913dup ENSP00000502579.1:p.Arg972GlufsTer27
ENST00000675517.1:c.3205dup
ENST00000676076.1:c.3191dup
ENST00000676260.1:c.3292dup
ENST00000676316.1:c.3217dup
ENST00000291825.11:c.*3535dup ENSP00000291825.6:n.*3535dup
ENST00000324001.7:c.3330dup ENSP00000326018.6:p.Arg1111GlufsTer27
NM_020956.2:c.*3535dup , LRG_265t1:c.*3535dup NP_066007.1:n.*3535dup
NM_181882.2:c.3330dup , LRG_265t2:c.3330dup NP_870998.2:p.Arg1111GlufsTer27
XM_011527171.1:c.3330dup XP_011525473.1:p.Arg1111GlufsTer27
XM_011527171.2:c.3330dup XP_011525473.1:p.Arg1111GlufsTer27
XM_017027046.1:c.3228dup XP_016882535.1:p.Arg1077GlufsTer27
XM_017027047.1:c.3228dup XP_016882536.1:p.Arg1077GlufsTer27
NM_181882.3:c.3330dup MANE Select NP_870998.2:p.Arg1111GlufsTer27