Canonical Allele Identifier: CA470163550
Gene: PLAU HGNC NCBI
C10orf55 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.75673111A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73913353A>G , CM000672.2:g.73913353A>G GRCh38
NC_000010.10:g.75673111A>G , CM000672.1:g.75673111A>G GRCh37
NC_000010.9:g.75343117A>G NCBI36
NG_011904.1:g.7250A>G , LRG_593:g.7250A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372764.4:c.432A>G (PLAU) MANE Select ENSP00000361850.3:p.Gln144=
ENST00000372764.3:c.432A>G (PLAU) ENSP00000361850.3:p.Gln144=
ENST00000409178.5:n.269-278T>C (C10orf55)
ENST00000412307.3:c.-73-278T>C (C10orf55) ENSP00000409225.2:n.-73-278T>C
ENST00000446342.5:c.381A>G (PLAU) ENSP00000388474.1:p.Gln127=
ENST00000494287.1:n.507A>G (PLAU)
NM_001001791.2:c.-73-278T>C (C10orf55) NP_001001791.2:n.-73-278T>C
NM_001145031.1:c.381A>G , LRG_593t2:c.381A>G (PLAU) NP_001138503.1:p.Gln127=
NM_002658.3:c.432A>G , LRG_593t1:c.432A>G (PLAU) NP_002649.1:p.Gln144=
XM_011539866.1:c.432A>G (PLAU) XP_011538168.1:p.Gln144=
XM_011539867.1:c.174A>G (PLAU) XP_011538169.1:p.Gln58=
NM_001145031.2:c.381A>G (PLAU) NP_001138503.1:p.Gln127=
NM_001319191.1:c.174A>G (PLAU) NP_001306120.1:p.Gln58=
NM_002658.4:c.432A>G (PLAU) NP_002649.1:p.Gln144=
XM_011539866.2:c.432A>G (PLAU) XP_011538168.1:p.Gln144=
NM_002658.5:c.432A>G (PLAU) NP_002649.1:p.Gln144=
NM_001145031.3:c.381A>G (PLAU) NP_001138503.2:p.Gln127=
NM_001319191.2:c.174A>G (PLAU) NP_001306120.2:p.Gln58=
NM_002658.6:c.432A>G (PLAU) MANE Select NP_002649.2:p.Gln144=
NR_160937.1:n.320-278T>C (C10orf55)
NR_160938.1:n.269-278T>C (C10orf55)