Canonical Allele Identifier: CA2585127083
Gene: PRX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40396208_40396209del , CM000681.2:g.40396208_40396209del GRCh38
NC_000019.9:g.40902115_40902116del , CM000681.1:g.40902115_40902116del GRCh37
NC_000019.8:g.45593955_45593956del NCBI36
NG_007979.1:g.22158_22159del , LRG_265:g.22158_22159del

Transcript Alleles

HGVS Amino-acid change
ENST00000324001.8:c.2145_2146del MANE Select ENSP00000326018.6:p.Cys715Ter
ENST00000673881.1:c.1728_1729del ENSP00000501070.1:p.Cys576Ter
ENST00000674005.2:c.2430_2431del ENSP00000501261.1:p.Cys810Ter
ENST00000674773.1:c.1728_1729del ENSP00000502579.1:p.Cys576Ter
ENST00000675517.1:c.2020_2021del
ENST00000676076.1:c.2006_2007del
ENST00000676260.1:c.2107_2108del
ENST00000676316.1:c.2032_2033del
ENST00000291825.11:c.*2350_*2351del ENSP00000291825.6:n.*2350_*2351del
ENST00000324001.7:c.2145_2146del ENSP00000326018.6:p.Cys715Ter
NM_020956.2:c.*2350_*2351del , LRG_265t1:c.*2350_*2351del NP_066007.1:n.*2350_*2351del
NM_181882.2:c.2145_2146del , LRG_265t2:c.2145_2146del NP_870998.2:p.Cys715Ter
XM_011527171.1:c.2145_2146del XP_011525473.1:p.Cys715Ter
XM_011527171.2:c.2145_2146del XP_011525473.1:p.Cys715Ter
XM_017027046.1:c.2043_2044del XP_016882535.1:p.Cys681Ter
XM_017027047.1:c.2043_2044del XP_016882536.1:p.Cys681Ter
NM_181882.3:c.2145_2146del MANE Select NP_870998.2:p.Cys715Ter