Canonical Allele Identifier: CA377254291

Gene: PLAU C10orf55

Linked Data

• MyVariant Identifiers: chr10:g.75673342G>T (hg19) ; chr10:g.73913584G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.73913584G>T , CM000672.2:g.73913584G>T	GRCh38
NC_000010.10:g.75673342G>T , CM000672.1:g.75673342G>T	GRCh37
NC_000010.9:g.75343348G>T	NCBI36
NG_011904.1:g.7481G>T , LRG_593:g.7481G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372764.4:c.506G>T (PLAU) MANE Select	ENSP00000361850.3:p.Gly169Val
ENST00000372764.3:c.506G>T (PLAU)	ENSP00000361850.3:p.Gly169Val
ENST00000409178.5:n.269-509C>A (C10orf55)
ENST00000412307.3:c.-73-509C>A (C10orf55)	ENSP00000409225.2:n.-73-509C>A
ENST00000446342.5:c.455G>T (PLAU)	ENSP00000388474.1:p.Gly152Val
ENST00000494287.1:n.581G>T (PLAU)
NM_001001791.2:c.-73-509C>A (C10orf55)	NP_001001791.2:n.-73-509C>A
NM_001145031.1:c.455G>T , LRG_593t2:c.455G>T (PLAU)	NP_001138503.1:p.Gly152Val
NM_002658.3:c.506G>T , LRG_593t1:c.506G>T (PLAU)	NP_002649.1:p.Gly169Val
XM_011539866.1:c.506G>T (PLAU)	XP_011538168.1:p.Gly169Val
XM_011539867.1:c.248G>T (PLAU)	XP_011538169.1:p.Gly83Val
NM_001145031.2:c.455G>T (PLAU)	NP_001138503.1:p.Gly152Val
NM_001319191.1:c.248G>T (PLAU)	NP_001306120.1:p.Gly83Val
NM_002658.4:c.506G>T (PLAU)	NP_002649.1:p.Gly169Val
XM_011539866.2:c.506G>T (PLAU)	XP_011538168.1:p.Gly169Val
NM_002658.5:c.506G>T (PLAU)	NP_002649.1:p.Gly169Val
NM_001145031.3:c.455G>T (PLAU)	NP_001138503.2:p.Gly152Val
NM_001319191.2:c.248G>T (PLAU)	NP_001306120.2:p.Gly83Val
NM_002658.6:c.506G>T (PLAU) MANE Select	NP_002649.2:p.Gly169Val
NR_160937.1:n.320-509C>A (C10orf55)
NR_160938.1:n.269-509C>A (C10orf55)