Canonical Allele Identifier: CA2335961575
Gene: PRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40396314G= , CM000681.2:g.40396314G= GRCh38
NC_000019.9:g.40902221G= , CM000681.1:g.40902221G= GRCh37
NC_000019.8:g.45594061G= NCBI36
NG_007979.1:g.22051C= , LRG_265:g.22051C=

Transcript Alleles

HGVS Amino-acid change
ENST00000324001.8:c.2038C= MANE Select ENSP00000326018.6:p.Leu680=
ENST00000673881.1:c.1621C= ENSP00000501070.1:p.Leu541=
ENST00000674005.2:c.2323C= ENSP00000501261.1:p.Leu775=
ENST00000674773.1:c.1621C= ENSP00000502579.1:p.Leu541=
ENST00000675517.1:c.1913C=
ENST00000676076.1:c.1899C=
ENST00000676260.1:c.2000C=
ENST00000676316.1:c.1925C=
ENST00000291825.11:c.*2243C= ENSP00000291825.6:n.*2243C=
ENST00000324001.7:c.2038C= ENSP00000326018.6:p.Leu680=
NM_020956.2:c.*2243C= , LRG_265t1:c.*2243C= NP_066007.1:n.*2243C=
NM_181882.2:c.2038C= , LRG_265t2:c.2038C= NP_870998.2:p.Leu680=
XM_011527171.1:c.2038C= XP_011525473.1:p.Leu680=
XM_011527171.2:c.2038C= XP_011525473.1:p.Leu680=
XM_017027046.1:c.1936C= XP_016882535.1:p.Leu646=
XM_017027047.1:c.1936C= XP_016882536.1:p.Leu646=
NM_181882.3:c.2038C= MANE Select NP_870998.2:p.Leu680=