Canonical Allele Identifier: CA5562573

Gene: PLAU C10orf55

Linked Data

• ClinVar Variation Id: 300757
• ClinVar RCV Id: RCV000308085 ; RCV001355163
• dbSNP Id: rs546931331
• ExAC: 10:75674582 G / A
• gnomAD v2: 10-75674582-G-A
• gnomAD v3: 10-73914824-G-A
• gnomAD v4: 10-73914824-G-A
• MyVariant Identifiers: chr10:g.75674582G>A (hg19) ; chr10:g.73914824G>A (hg38)
• PubMed: PMID:28135719

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.73914824G>A , CM000672.2:g.73914824G>A	GRCh38
NC_000010.10:g.75674582G>A , CM000672.1:g.75674582G>A	GRCh37
NC_000010.9:g.75344588G>A	NCBI36
NG_011904.1:g.8721G>A , LRG_593:g.8721G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000372764.4:c.878G>A (PLAU) MANE Select	ENSP00000361850.3:p.Arg293Gln
ENST00000372764.3:c.878G>A (PLAU)	ENSP00000361850.3:p.Arg293Gln
ENST00000409178.5:n.268+1695C>T (C10orf55)
ENST00000412307.3:c.-74+1695C>T (C10orf55)	ENSP00000409225.2:n.-74+1695C>T
ENST00000446342.5:c.827G>A (PLAU)	ENSP00000388474.1:p.Arg276Gln
NM_001001791.2:c.-74+1695C>T (C10orf55)	NP_001001791.2:n.-74+1695C>T
NM_001145031.1:c.827G>A , LRG_593t2:c.827G>A (PLAU)	NP_001138503.1:p.Arg276Gln
NM_002658.3:c.878G>A , LRG_593t1:c.878G>A (PLAU)	NP_002649.1:p.Arg293Gln
XM_011539866.1:c.878G>A (PLAU)	XP_011538168.1:p.Arg293Gln
XM_011539867.1:c.620G>A (PLAU)	XP_011538169.1:p.Arg207Gln
NM_001145031.2:c.827G>A (PLAU)	NP_001138503.1:p.Arg276Gln
NM_001319191.1:c.620G>A (PLAU)	NP_001306120.1:p.Arg207Gln
NM_002658.4:c.878G>A (PLAU)	NP_002649.1:p.Arg293Gln
XM_011539866.2:c.878G>A (PLAU)	XP_011538168.1:p.Arg293Gln
NM_002658.5:c.878G>A (PLAU)	NP_002649.1:p.Arg293Gln
NM_001145031.3:c.827G>A (PLAU)	NP_001138503.2:p.Arg276Gln
NM_001319191.2:c.620G>A (PLAU)	NP_001306120.2:p.Arg207Gln
NM_002658.6:c.878G>A (PLAU) MANE Select	NP_002649.2:p.Arg293Gln
NR_160937.1:n.319+747C>T (C10orf55)
NR_160938.1:n.268+1695C>T (C10orf55)