Canonical Allele Identifier: CA2335961474
Gene: PRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40396123G= , CM000681.2:g.40396123G= GRCh38
NC_000019.9:g.40902030G= , CM000681.1:g.40902030G= GRCh37
NC_000019.8:g.45593870G= NCBI36
NG_007979.1:g.22242C= , LRG_265:g.22242C=

Transcript Alleles

HGVS Amino-acid change
ENST00000324001.8:c.2229C= MANE Select ENSP00000326018.6:p.Pro743=
ENST00000673881.1:c.1812C= ENSP00000501070.1:p.Pro604=
ENST00000674005.2:c.2514C= ENSP00000501261.1:p.Pro838=
ENST00000674773.1:c.1812C= ENSP00000502579.1:p.Pro604=
ENST00000675517.1:c.2104C=
ENST00000676076.1:c.2090C=
ENST00000676260.1:c.2191C=
ENST00000676316.1:c.2116C=
ENST00000291825.11:c.*2434C= ENSP00000291825.6:n.*2434C=
ENST00000324001.7:c.2229C= ENSP00000326018.6:p.Pro743=
NM_020956.2:c.*2434C= , LRG_265t1:c.*2434C= NP_066007.1:n.*2434C=
NM_181882.2:c.2229C= , LRG_265t2:c.2229C= NP_870998.2:p.Pro743=
XM_011527171.1:c.2229C= XP_011525473.1:p.Pro743=
XM_011527171.2:c.2229C= XP_011525473.1:p.Pro743=
XM_017027046.1:c.2127C= XP_016882535.1:p.Pro709=
XM_017027047.1:c.2127C= XP_016882536.1:p.Pro709=
NM_181882.3:c.2229C= MANE Select NP_870998.2:p.Pro743=