Canonical Allele Identifier: CA5562667

Gene: PLAU C10orf55

Linked Data

• ClinVar Variation Id: 1029617
• ClinVar RCV Id: RCV001330951
• dbSNP Id: rs764252595
• ExAC: 10:75676256 C / T
• gnomAD v2: 10-75676256-C-T
• gnomAD v3: 10-73916498-C-T
• gnomAD v4: 10-73916498-C-T
• MyVariant Identifiers: chr10:g.75676256C>T (hg19) ; chr10:g.73916498C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.73916498C>T , CM000672.2:g.73916498C>T	GRCh38
NC_000010.10:g.75676256C>T , CM000672.1:g.75676256C>T	GRCh37
NC_000010.9:g.75346262C>T	NCBI36
NG_011904.1:g.10395C>T , LRG_593:g.10395C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372764.4:c.1229C>T (PLAU) MANE Select	ENSP00000361850.3:p.Thr410Met
ENST00000372764.3:c.1229C>T (PLAU)	ENSP00000361850.3:p.Thr410Met
ENST00000409178.5:n.268+21G>A (C10orf55)
ENST00000412307.3:c.-74+21G>A (C10orf55)	ENSP00000409225.2:n.-74+21G>A
ENST00000446342.5:c.1178C>T (PLAU)	ENSP00000388474.1:p.Thr393Met
NM_001001791.2:c.-74+21G>A (C10orf55)	NP_001001791.2:n.-74+21G>A
NM_001145031.1:c.1178C>T , LRG_593t2:c.1178C>T (PLAU)	NP_001138503.1:p.Thr393Met
NM_002658.3:c.1229C>T , LRG_593t1:c.1229C>T (PLAU)	NP_002649.1:p.Thr410Met
XM_011539866.1:c.1229C>T (PLAU)	XP_011538168.1:p.Thr410Met
XM_011539867.1:c.971C>T (PLAU)	XP_011538169.1:p.Thr324Met
NM_001145031.2:c.1178C>T (PLAU)	NP_001138503.1:p.Thr393Met
NM_001319191.1:c.971C>T (PLAU)	NP_001306120.1:p.Thr324Met
NM_002658.4:c.1229C>T (PLAU)	NP_002649.1:p.Thr410Met
XM_011539866.2:c.1229C>T (PLAU)	XP_011538168.1:p.Thr410Met
NM_002658.5:c.1229C>T (PLAU)	NP_002649.1:p.Thr410Met
NM_001145031.3:c.1178C>T (PLAU)	NP_001138503.2:p.Thr393Met
NM_001319191.2:c.971C>T (PLAU)	NP_001306120.2:p.Thr324Met
NM_002658.6:c.1229C>T (PLAU) MANE Select	NP_002649.2:p.Thr410Met
NR_160937.1:n.268+21G>A (C10orf55)
NR_160938.1:n.268+21G>A (C10orf55)