Canonical Allele Identifier: CA507679437
Gene: PRX HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.40901940C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40396033C>T , CM000681.2:g.40396033C>T GRCh38
NC_000019.9:g.40901940C>T , CM000681.1:g.40901940C>T GRCh37
NC_000019.8:g.45593780C>T NCBI36
NG_007979.1:g.22332G>A , LRG_265:g.22332G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324001.8:c.2319G>A MANE Select ENSP00000326018.6:p.Glu773=
ENST00000673881.1:c.1902G>A ENSP00000501070.1:p.Glu634=
ENST00000674005.2:c.2604G>A ENSP00000501261.1:p.Glu868=
ENST00000674773.1:c.1902G>A ENSP00000502579.1:p.Glu634=
ENST00000675517.1:c.2194G>A
ENST00000676076.1:c.2180G>A
ENST00000676260.1:c.2281G>A
ENST00000676316.1:c.2206G>A
ENST00000291825.11:c.*2524G>A ENSP00000291825.6:n.*2524G>A
ENST00000324001.7:c.2319G>A ENSP00000326018.6:p.Glu773=
NM_020956.2:c.*2524G>A , LRG_265t1:c.*2524G>A NP_066007.1:n.*2524G>A
NM_181882.2:c.2319G>A , LRG_265t2:c.2319G>A NP_870998.2:p.Glu773=
XM_011527171.1:c.2319G>A XP_011525473.1:p.Glu773=
XM_011527171.2:c.2319G>A XP_011525473.1:p.Glu773=
XM_017027046.1:c.2217G>A XP_016882535.1:p.Glu739=
XM_017027047.1:c.2217G>A XP_016882536.1:p.Glu739=
NM_181882.3:c.2319G>A MANE Select NP_870998.2:p.Glu773=