Canonical Allele Identifier: CA5562685

Gene: PLAU C10orf55

Linked Data

• ClinVar Variation Id: 300763
• ClinVar RCV Id: RCV000315536
• dbSNP Id: rs560674195
• ExAC: 10:75676375 T / A
• gnomAD v2: 10-75676375-T-A
• gnomAD v3: 10-73916617-T-A
• gnomAD v4: 10-73916617-T-A
• MyVariant Identifiers: chr10:g.75676375T>A (hg19) ; chr10:g.73916617T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.73916617T>A , CM000672.2:g.73916617T>A	GRCh38
NC_000010.10:g.75676375T>A , CM000672.1:g.75676375T>A	GRCh37
NC_000010.9:g.75346381T>A	NCBI36
NG_011904.1:g.10514T>A , LRG_593:g.10514T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372764.4:c.*52T>A (PLAU) MANE Select	ENSP00000361850.3:n.*52T>A
ENST00000372764.3:c.*52T>A (PLAU)	ENSP00000361850.3:n.*52T>A
ENST00000409178.5:n.170A>T (C10orf55)
ENST00000412307.3:c.-172A>T (C10orf55)	ENSP00000409225.2:n.-172A>T
ENST00000446342.5:c.*52T>A (PLAU)	ENSP00000388474.1:n.*52T>A
NM_001001791.2:c.-172A>T (C10orf55)	NP_001001791.2:n.-172A>T
NM_001145031.1:c.*52T>A , LRG_593t2:c.*52T>A (PLAU)	NP_001138503.1:n.*52T>A
NM_002658.3:c.*52T>A , LRG_593t1:c.*52T>A (PLAU)	NP_002649.1:n.*52T>A
XM_011539866.1:c.*52T>A (PLAU)	XP_011538168.1:n.*52T>A
XM_011539867.1:c.*52T>A (PLAU)	XP_011538169.1:n.*52T>A
NM_001145031.2:c.*52T>A (PLAU)	NP_001138503.1:n.*52T>A
NM_001319191.1:c.*52T>A (PLAU)	NP_001306120.1:n.*52T>A
NM_002658.4:c.*52T>A (PLAU)	NP_002649.1:n.*52T>A
XM_011539866.2:c.*52T>A (PLAU)	XP_011538168.1:n.*52T>A
NM_002658.5:c.*52T>A (PLAU)	NP_002649.1:n.*52T>A
NM_001145031.3:c.*52T>A (PLAU)	NP_001138503.2:n.*52T>A
NM_001319191.2:c.*52T>A (PLAU)	NP_001306120.2:n.*52T>A
NM_002658.6:c.*52T>A (PLAU) MANE Select	NP_002649.2:n.*52T>A
NR_160937.1:n.170A>T (C10orf55)
NR_160938.1:n.170A>T (C10orf55)