Canonical Allele Identifier: CA1919822131
Gene: PLAU HGNC NCBI
C10orf55 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73916654A= , CM000672.2:g.73916654A= GRCh38
NC_000010.10:g.75676412A= , CM000672.1:g.75676412A= GRCh37
NC_000010.9:g.75346418A= NCBI36
NG_011904.1:g.10551A= , LRG_593:g.10551A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372764.4:c.*89A= (PLAU) MANE Select ENSP00000361850.3:n.*89A=
ENST00000372764.3:c.*89A= (PLAU) ENSP00000361850.3:n.*89A=
ENST00000409178.5:n.146-13T= (C10orf55)
ENST00000446342.5:c.*89A= (PLAU) ENSP00000388474.1:n.*89A=
NM_001001791.2:c.-196-13T= (C10orf55) NP_001001791.2:n.-196-13T=
NM_001145031.1:c.*89A= , LRG_593t2:c.*89A= (PLAU) NP_001138503.1:n.*89A=
NM_002658.3:c.*89A= , LRG_593t1:c.*89A= (PLAU) NP_002649.1:n.*89A=
XM_011539866.1:c.*89A= (PLAU) XP_011538168.1:n.*89A=
XM_011539867.1:c.*89A= (PLAU) XP_011538169.1:n.*89A=
NM_001145031.2:c.*89A= (PLAU) NP_001138503.1:n.*89A=
NM_001319191.1:c.*89A= (PLAU) NP_001306120.1:n.*89A=
NM_002658.4:c.*89A= (PLAU) NP_002649.1:n.*89A=
XM_011539866.2:c.*89A= (PLAU) XP_011538168.1:n.*89A=
NM_002658.5:c.*89A= (PLAU) NP_002649.1:n.*89A=
NM_001145031.3:c.*89A= (PLAU) NP_001138503.2:n.*89A=
NM_001319191.2:c.*89A= (PLAU) NP_001306120.2:n.*89A=
NM_002658.6:c.*89A= (PLAU) MANE Select NP_002649.2:n.*89A=
NR_160937.1:n.146-13T= (C10orf55)
NR_160938.1:n.146-13T= (C10orf55)