Canonical Allele Identifier: CA5562671

Gene: PLAU C10orf55

Linked Data

• dbSNP Id: rs746212195
• ExAC: 10:75676267 C / T
• gnomAD v2: 10-75676267-C-T
• gnomAD v3: 10-73916509-C-T
• gnomAD v4: 10-73916509-C-T
• MyVariant Identifiers: chr10:g.75676267C>T (hg19) ; chr10:g.73916509C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.73916509C>T , CM000672.2:g.73916509C>T	GRCh38
NC_000010.10:g.75676267C>T , CM000672.1:g.75676267C>T	GRCh37
NC_000010.9:g.75346273C>T	NCBI36
NG_011904.1:g.10406C>T , LRG_593:g.10406C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372764.4:c.1240C>T (PLAU) MANE Select	ENSP00000361850.3:p.His414Tyr
ENST00000372764.3:c.1240C>T (PLAU)	ENSP00000361850.3:p.His414Tyr
ENST00000409178.5:n.268+10G>A (C10orf55)
ENST00000412307.3:c.-74+10G>A (C10orf55)	ENSP00000409225.2:n.-74+10G>A
ENST00000446342.5:c.1189C>T (PLAU)	ENSP00000388474.1:p.His397Tyr
NM_001001791.2:c.-74+10G>A (C10orf55)	NP_001001791.2:n.-74+10G>A
NM_001145031.1:c.1189C>T , LRG_593t2:c.1189C>T (PLAU)	NP_001138503.1:p.His397Tyr
NM_002658.3:c.1240C>T , LRG_593t1:c.1240C>T (PLAU)	NP_002649.1:p.His414Tyr
XM_011539866.1:c.1240C>T (PLAU)	XP_011538168.1:p.His414Tyr
XM_011539867.1:c.982C>T (PLAU)	XP_011538169.1:p.His328Tyr
NM_001145031.2:c.1189C>T (PLAU)	NP_001138503.1:p.His397Tyr
NM_001319191.1:c.982C>T (PLAU)	NP_001306120.1:p.His328Tyr
NM_002658.4:c.1240C>T (PLAU)	NP_002649.1:p.His414Tyr
XM_011539866.2:c.1240C>T (PLAU)	XP_011538168.1:p.His414Tyr
NM_002658.5:c.1240C>T (PLAU)	NP_002649.1:p.His414Tyr
NM_001145031.3:c.1189C>T (PLAU)	NP_001138503.2:p.His397Tyr
NM_001319191.2:c.982C>T (PLAU)	NP_001306120.2:p.His328Tyr
NM_002658.6:c.1240C>T (PLAU) MANE Select	NP_002649.2:p.His414Tyr
NR_160937.1:n.268+10G>A (C10orf55)
NR_160938.1:n.268+10G>A (C10orf55)