Canonical Allele Identifier: CA405896802
Gene: PRX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40396160T>A , CM000681.2:g.40396160T>A GRCh38
NC_000019.9:g.40902067T>A , CM000681.1:g.40902067T>A GRCh37
NC_000019.8:g.45593907T>A NCBI36
NG_007979.1:g.22205A>T , LRG_265:g.22205A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000324001.8:c.2192A>T MANE Select ENSP00000326018.6:p.Lys731Met
ENST00000673881.1:c.1775A>T ENSP00000501070.1:p.Lys592Met
ENST00000674005.2:c.2477A>T ENSP00000501261.1:p.Lys826Met
ENST00000674773.1:c.1775A>T ENSP00000502579.1:p.Lys592Met
ENST00000675517.1:c.2067A>T
ENST00000676076.1:c.2053A>T
ENST00000676260.1:c.2154A>T
ENST00000676316.1:c.2079A>T
ENST00000291825.11:c.*2397A>T ENSP00000291825.6:n.*2397A>T
ENST00000324001.7:c.2192A>T ENSP00000326018.6:p.Lys731Met
NM_020956.2:c.*2397A>T , LRG_265t1:c.*2397A>T NP_066007.1:n.*2397A>T
NM_181882.2:c.2192A>T , LRG_265t2:c.2192A>T NP_870998.2:p.Lys731Met
XM_011527171.1:c.2192A>T XP_011525473.1:p.Lys731Met
XM_011527171.2:c.2192A>T XP_011525473.1:p.Lys731Met
XM_017027046.1:c.2090A>T XP_016882535.1:p.Lys697Met
XM_017027047.1:c.2090A>T XP_016882536.1:p.Lys697Met
NM_181882.3:c.2192A>T MANE Select NP_870998.2:p.Lys731Met