Canonical Allele Identifier: CA377259708
Gene: PLAU HGNC NCBI
C10orf55 HGNC NCBI

Linked Data

COSMIC: COSM685325

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73916501G>C , CM000672.2:g.73916501G>C GRCh38
NC_000010.10:g.75676259G>C , CM000672.1:g.75676259G>C GRCh37
NC_000010.9:g.75346265G>C NCBI36
NG_011904.1:g.10398G>C , LRG_593:g.10398G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372764.4:c.1232G>C (PLAU) MANE Select ENSP00000361850.3:p.Arg411Thr
ENST00000372764.3:c.1232G>C (PLAU) ENSP00000361850.3:p.Arg411Thr
ENST00000409178.5:n.268+18C>G (C10orf55)
ENST00000412307.3:c.-74+18C>G (C10orf55) ENSP00000409225.2:n.-74+18C>G
ENST00000446342.5:c.1181G>C (PLAU) ENSP00000388474.1:p.Arg394Thr
NM_001001791.2:c.-74+18C>G (C10orf55) NP_001001791.2:n.-74+18C>G
NM_001145031.1:c.1181G>C , LRG_593t2:c.1181G>C (PLAU) NP_001138503.1:p.Arg394Thr
NM_002658.3:c.1232G>C , LRG_593t1:c.1232G>C (PLAU) NP_002649.1:p.Arg411Thr
XM_011539866.1:c.1232G>C (PLAU) XP_011538168.1:p.Arg411Thr
XM_011539867.1:c.974G>C (PLAU) XP_011538169.1:p.Arg325Thr
NM_001145031.2:c.1181G>C (PLAU) NP_001138503.1:p.Arg394Thr
NM_001319191.1:c.974G>C (PLAU) NP_001306120.1:p.Arg325Thr
NM_002658.4:c.1232G>C (PLAU) NP_002649.1:p.Arg411Thr
XM_011539866.2:c.1232G>C (PLAU) XP_011538168.1:p.Arg411Thr
NM_002658.5:c.1232G>C (PLAU) NP_002649.1:p.Arg411Thr
NM_001145031.3:c.1181G>C (PLAU) NP_001138503.2:p.Arg394Thr
NM_001319191.2:c.974G>C (PLAU) NP_001306120.2:p.Arg325Thr
NM_002658.6:c.1232G>C (PLAU) MANE Select NP_002649.2:p.Arg411Thr
NR_160937.1:n.268+18C>G (C10orf55)
NR_160938.1:n.268+18C>G (C10orf55)