Canonical Allele Identifier: CA470163126
Gene: PLAU HGNC NCBI
C10orf55 HGNC NCBI

Linked Data

dbSNP Id: rs149099771
MyVariant Identifiers: chr10:g.75672839G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73913081G>T , CM000672.2:g.73913081G>T GRCh38
NC_000010.10:g.75672839G>T , CM000672.1:g.75672839G>T GRCh37
NC_000010.9:g.75342845G>T NCBI36
NG_011904.1:g.6978G>T , LRG_593:g.6978G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372764.4:c.351G>T (PLAU) MANE Select ENSP00000361850.3:p.Gly117=
ENST00000372764.3:c.351G>T (PLAU) ENSP00000361850.3:p.Gly117=
ENST00000409178.5:n.269-6C>A (C10orf55)
ENST00000412307.3:c.-73-6C>A (C10orf55) ENSP00000409225.2:n.-73-6C>A
ENST00000446342.5:c.300G>T (PLAU) ENSP00000388474.1:p.Gly100=
ENST00000494287.1:n.426G>T (PLAU)
NM_001001791.2:c.-73-6C>A (C10orf55) NP_001001791.2:n.-73-6C>A
NM_001145031.1:c.300G>T , LRG_593t2:c.300G>T (PLAU) NP_001138503.1:p.Gly100=
NM_002658.3:c.351G>T , LRG_593t1:c.351G>T (PLAU) NP_002649.1:p.Gly117=
XM_011539866.1:c.351G>T (PLAU) XP_011538168.1:p.Gly117=
XM_011539867.1:c.93G>T (PLAU) XP_011538169.1:p.Gly31=
NM_001145031.2:c.300G>T (PLAU) NP_001138503.1:p.Gly100=
NM_001319191.1:c.93G>T (PLAU) NP_001306120.1:p.Gly31=
NM_002658.4:c.351G>T (PLAU) NP_002649.1:p.Gly117=
XM_011539866.2:c.351G>T (PLAU) XP_011538168.1:p.Gly117=
NM_002658.5:c.351G>T (PLAU) NP_002649.1:p.Gly117=
NM_001145031.3:c.300G>T (PLAU) NP_001138503.2:p.Gly100=
NM_001319191.2:c.93G>T (PLAU) NP_001306120.2:p.Gly31=
NM_002658.6:c.351G>T (PLAU) MANE Select NP_002649.2:p.Gly117=
NR_160937.1:n.320-6C>A (C10orf55)
NR_160938.1:n.269-6C>A (C10orf55)