Canonical Allele Identifier: CA405897351
Gene: PRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40396416C>G , CM000681.2:g.40396416C>G GRCh38
NC_000019.9:g.40902323C>G , CM000681.1:g.40902323C>G GRCh37
NC_000019.8:g.45594163C>G NCBI36
NG_007979.1:g.21949G>C , LRG_265:g.21949G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324001.8:c.1936G>C MANE Select ENSP00000326018.6:p.Glu646Gln
ENST00000673881.1:c.1519G>C ENSP00000501070.1:p.Glu507Gln
ENST00000674005.2:c.2221G>C ENSP00000501261.1:p.Glu741Gln
ENST00000674773.1:c.1519G>C ENSP00000502579.1:p.Glu507Gln
ENST00000675517.1:c.1811G>C
ENST00000676076.1:c.1797G>C
ENST00000676260.1:c.1898G>C
ENST00000676316.1:c.1823G>C
ENST00000291825.11:c.*2141G>C ENSP00000291825.6:n.*2141G>C
ENST00000324001.7:c.1936G>C ENSP00000326018.6:p.Glu646Gln
NM_020956.2:c.*2141G>C , LRG_265t1:c.*2141G>C NP_066007.1:n.*2141G>C
NM_181882.2:c.1936G>C , LRG_265t2:c.1936G>C NP_870998.2:p.Glu646Gln
XM_011527171.1:c.1936G>C XP_011525473.1:p.Glu646Gln
XM_011527171.2:c.1936G>C XP_011525473.1:p.Glu646Gln
XM_017027046.1:c.1834G>C XP_016882535.1:p.Glu612Gln
XM_017027047.1:c.1834G>C XP_016882536.1:p.Glu612Gln
NM_181882.3:c.1936G>C MANE Select NP_870998.2:p.Glu646Gln