Canonical Allele Identifier: CA2335961577
Gene: PRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40396317G= , CM000681.2:g.40396317G= GRCh38
NC_000019.9:g.40902224G= , CM000681.1:g.40902224G= GRCh37
NC_000019.8:g.45594064G= NCBI36
NG_007979.1:g.22048C= , LRG_265:g.22048C=

Transcript Alleles

HGVS Amino-acid change
ENST00000324001.8:c.2035C= MANE Select ENSP00000326018.6:p.Arg679=
ENST00000673881.1:c.1618C= ENSP00000501070.1:p.Arg540=
ENST00000674005.2:c.2320C= ENSP00000501261.1:p.Arg774=
ENST00000674773.1:c.1618C= ENSP00000502579.1:p.Arg540=
ENST00000675517.1:c.1910C=
ENST00000676076.1:c.1896C=
ENST00000676260.1:c.1997C=
ENST00000676316.1:c.1922C=
ENST00000291825.11:c.*2240C= ENSP00000291825.6:n.*2240C=
ENST00000324001.7:c.2035C= ENSP00000326018.6:p.Arg679=
NM_020956.2:c.*2240C= , LRG_265t1:c.*2240C= NP_066007.1:n.*2240C=
NM_181882.2:c.2035C= , LRG_265t2:c.2035C= NP_870998.2:p.Arg679=
XM_011527171.1:c.2035C= XP_011525473.1:p.Arg679=
XM_011527171.2:c.2035C= XP_011525473.1:p.Arg679=
XM_017027046.1:c.1933C= XP_016882535.1:p.Arg645=
XM_017027047.1:c.1933C= XP_016882536.1:p.Arg645=
NM_181882.3:c.2035C= MANE Select NP_870998.2:p.Arg679=