Canonical Allele Identifier: CA594709281

Gene: PLAU C10orf55

Linked Data

• ClinVar Variation Id: 1696678
• ClinVar RCV Id: RCV002266808
• dbSNP Id: rs1435611170
• gnomAD v2: 10-75673297-G-GA
• gnomAD v3: 10-73913539-G-GA
• gnomAD v4: 10-73913539-G-GA
• MyVariant Identifiers: chr10:g.75673297_75673298insA (hg19) ; chr10:g.73913539_73913540insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.73913545dup , CM000672.2:g.73913545dup	GRCh38
NC_000010.10:g.75673303dup , CM000672.1:g.75673303dup	GRCh37
NC_000010.9:g.75343309dup	NCBI36
NG_011904.1:g.7442dup , LRG_593:g.7442dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372764.4:c.467dup (PLAU) MANE Select	ENSP00000361850.3:p.Pro157AlafsTer22
ENST00000372764.3:c.467dup (PLAU)	ENSP00000361850.3:p.Pro157AlafsTer22
ENST00000409178.5:n.269-465dup (C10orf55)
ENST00000412307.3:c.-73-465dup (C10orf55)	ENSP00000409225.2:n.-73-465dup
ENST00000446342.5:c.416dup (PLAU)	ENSP00000388474.1:p.Pro140AlafsTer22
ENST00000494287.1:n.542dup (PLAU)
NM_001001791.2:c.-73-465dup (C10orf55)	NP_001001791.2:n.-73-465dup
NM_001145031.1:c.416dup , LRG_593t2:c.416dup (PLAU)	NP_001138503.1:p.Pro140AlafsTer22
NM_002658.3:c.467dup , LRG_593t1:c.467dup (PLAU)	NP_002649.1:p.Pro157AlafsTer22
XM_011539866.1:c.467dup (PLAU)	XP_011538168.1:p.Pro157AlafsTer22
XM_011539867.1:c.209dup (PLAU)	XP_011538169.1:p.Pro71AlafsTer22
NM_001145031.2:c.416dup (PLAU)	NP_001138503.1:p.Pro140AlafsTer22
NM_001319191.1:c.209dup (PLAU)	NP_001306120.1:p.Pro71AlafsTer22
NM_002658.4:c.467dup (PLAU)	NP_002649.1:p.Pro157AlafsTer22
XM_011539866.2:c.467dup (PLAU)	XP_011538168.1:p.Pro157AlafsTer22
NM_002658.5:c.467dup (PLAU)	NP_002649.1:p.Pro157AlafsTer22
NM_001145031.3:c.416dup (PLAU)	NP_001138503.2:p.Pro140AlafsTer22
NM_001319191.2:c.209dup (PLAU)	NP_001306120.2:p.Pro71AlafsTer22
NM_002658.6:c.467dup (PLAU) MANE Select	NP_002649.2:p.Pro157AlafsTer22
NR_160937.1:n.320-465dup (C10orf55)
NR_160938.1:n.269-465dup (C10orf55)