Canonical Allele Identifier: CA1919822070
Gene: PLAU HGNC NCBI
C10orf55 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73916498C= , CM000672.2:g.73916498C= GRCh38
NC_000010.10:g.75676256C= , CM000672.1:g.75676256C= GRCh37
NC_000010.9:g.75346262C= NCBI36
NG_011904.1:g.10395C= , LRG_593:g.10395C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372764.4:c.1229C= (PLAU) MANE Select ENSP00000361850.3:p.Thr410=
ENST00000372764.3:c.1229C= (PLAU) ENSP00000361850.3:p.Thr410=
ENST00000409178.5:n.268+21G= (C10orf55)
ENST00000412307.3:c.-74+21G= (C10orf55) ENSP00000409225.2:n.-74+21G=
ENST00000446342.5:c.1178C= (PLAU) ENSP00000388474.1:p.Thr393=
NM_001001791.2:c.-74+21G= (C10orf55) NP_001001791.2:n.-74+21G=
NM_001145031.1:c.1178C= , LRG_593t2:c.1178C= (PLAU) NP_001138503.1:p.Thr393=
NM_002658.3:c.1229C= , LRG_593t1:c.1229C= (PLAU) NP_002649.1:p.Thr410=
XM_011539866.1:c.1229C= (PLAU) XP_011538168.1:p.Thr410=
XM_011539867.1:c.971C= (PLAU) XP_011538169.1:p.Thr324=
NM_001145031.2:c.1178C= (PLAU) NP_001138503.1:p.Thr393=
NM_001319191.1:c.971C= (PLAU) NP_001306120.1:p.Thr324=
NM_002658.4:c.1229C= (PLAU) NP_002649.1:p.Thr410=
XM_011539866.2:c.1229C= (PLAU) XP_011538168.1:p.Thr410=
NM_002658.5:c.1229C= (PLAU) NP_002649.1:p.Thr410=
NM_001145031.3:c.1178C= (PLAU) NP_001138503.2:p.Thr393=
NM_001319191.2:c.971C= (PLAU) NP_001306120.2:p.Thr324=
NM_002658.6:c.1229C= (PLAU) MANE Select NP_002649.2:p.Thr410=
NR_160937.1:n.268+21G= (C10orf55)
NR_160938.1:n.268+21G= (C10orf55)