Canonical Allele Identifier: CA5562457

Gene: PLAU C10orf55

Linked Data

• ClinVar Variation Id: 2582777
• ClinVar RCV Id: RCV003333893 ; RCV004334122
• dbSNP Id: rs771200321
• ExAC: 10:75673375 T / C
• gnomAD v2: 10-75673375-T-C
• gnomAD v3: 10-73913617-T-C
• gnomAD v4: 10-73913617-T-C
• MyVariant Identifiers: chr10:g.75673375T>C (hg19) ; chr10:g.73913617T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.73913617T>C , CM000672.2:g.73913617T>C	GRCh38
NC_000010.10:g.75673375T>C , CM000672.1:g.75673375T>C	GRCh37
NC_000010.9:g.75343381T>C	NCBI36
NG_011904.1:g.7514T>C , LRG_593:g.7514T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372764.4:c.539T>C (PLAU) MANE Select	ENSP00000361850.3:p.Ile180Thr
ENST00000372764.3:c.539T>C (PLAU)	ENSP00000361850.3:p.Ile180Thr
ENST00000409178.5:n.269-542A>G (C10orf55)
ENST00000412307.3:c.-73-542A>G (C10orf55)	ENSP00000409225.2:n.-73-542A>G
ENST00000446342.5:c.488T>C (PLAU)	ENSP00000388474.1:p.Ile163Thr
ENST00000494287.1:n.614T>C (PLAU)
NM_001001791.2:c.-73-542A>G (C10orf55)	NP_001001791.2:n.-73-542A>G
NM_001145031.1:c.488T>C , LRG_593t2:c.488T>C (PLAU)	NP_001138503.1:p.Ile163Thr
NM_002658.3:c.539T>C , LRG_593t1:c.539T>C (PLAU)	NP_002649.1:p.Ile180Thr
XM_011539866.1:c.539T>C (PLAU)	XP_011538168.1:p.Ile180Thr
XM_011539867.1:c.281T>C (PLAU)	XP_011538169.1:p.Ile94Thr
NM_001145031.2:c.488T>C (PLAU)	NP_001138503.1:p.Ile163Thr
NM_001319191.1:c.281T>C (PLAU)	NP_001306120.1:p.Ile94Thr
NM_002658.4:c.539T>C (PLAU)	NP_002649.1:p.Ile180Thr
XM_011539866.2:c.539T>C (PLAU)	XP_011538168.1:p.Ile180Thr
NM_002658.5:c.539T>C (PLAU)	NP_002649.1:p.Ile180Thr
NM_001145031.3:c.488T>C (PLAU)	NP_001138503.2:p.Ile163Thr
NM_001319191.2:c.281T>C (PLAU)	NP_001306120.2:p.Ile94Thr
NM_002658.6:c.539T>C (PLAU) MANE Select	NP_002649.2:p.Ile180Thr
NR_160937.1:n.320-542A>G (C10orf55)
NR_160938.1:n.269-542A>G (C10orf55)