Canonical Allele Identifier: CA470163844
Gene: PLAU HGNC NCBI
C10orf55 HGNC NCBI

Linked Data

dbSNP Id: rs2096129625
MyVariant Identifiers: chr10:g.75673376T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73913618T>C , CM000672.2:g.73913618T>C GRCh38
NC_000010.10:g.75673376T>C , CM000672.1:g.75673376T>C GRCh37
NC_000010.9:g.75343382T>C NCBI36
NG_011904.1:g.7515T>C , LRG_593:g.7515T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372764.4:c.540T>C (PLAU) MANE Select ENSP00000361850.3:p.Ile180=
ENST00000372764.3:c.540T>C (PLAU) ENSP00000361850.3:p.Ile180=
ENST00000409178.5:n.269-543A>G (C10orf55)
ENST00000412307.3:c.-73-543A>G (C10orf55) ENSP00000409225.2:n.-73-543A>G
ENST00000446342.5:c.489T>C (PLAU) ENSP00000388474.1:p.Ile163=
ENST00000494287.1:n.615T>C (PLAU)
NM_001001791.2:c.-73-543A>G (C10orf55) NP_001001791.2:n.-73-543A>G
NM_001145031.1:c.489T>C , LRG_593t2:c.489T>C (PLAU) NP_001138503.1:p.Ile163=
NM_002658.3:c.540T>C , LRG_593t1:c.540T>C (PLAU) NP_002649.1:p.Ile180=
XM_011539866.1:c.540T>C (PLAU) XP_011538168.1:p.Ile180=
XM_011539867.1:c.282T>C (PLAU) XP_011538169.1:p.Ile94=
NM_001145031.2:c.489T>C (PLAU) NP_001138503.1:p.Ile163=
NM_001319191.1:c.282T>C (PLAU) NP_001306120.1:p.Ile94=
NM_002658.4:c.540T>C (PLAU) NP_002649.1:p.Ile180=
XM_011539866.2:c.540T>C (PLAU) XP_011538168.1:p.Ile180=
NM_002658.5:c.540T>C (PLAU) NP_002649.1:p.Ile180=
NM_001145031.3:c.489T>C (PLAU) NP_001138503.2:p.Ile163=
NM_001319191.2:c.282T>C (PLAU) NP_001306120.2:p.Ile94=
NM_002658.6:c.540T>C (PLAU) MANE Select NP_002649.2:p.Ile180=
NR_160937.1:n.320-543A>G (C10orf55)
NR_160938.1:n.269-543A>G (C10orf55)