Canonical Allele Identifier: CA5562607
Gene: PLAU HGNC NCBI
C10orf55 HGNC NCBI

Linked Data

ClinVar Variation Id: 300758
dbSNP Id: rs72816325

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73915328T>C , CM000672.2:g.73915328T>C GRCh38
NC_000010.10:g.75675086T>C , CM000672.1:g.75675086T>C GRCh37
NC_000010.9:g.75345092T>C NCBI36
NG_011904.1:g.9225T>C , LRG_593:g.9225T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372764.4:c.1048T>C (PLAU) MANE Select ENSP00000361850.3:p.Tyr350His
ENST00000372764.3:c.1048T>C (PLAU) ENSP00000361850.3:p.Tyr350His
ENST00000409178.5:n.268+1191A>G (C10orf55)
ENST00000412307.3:c.-74+1191A>G (C10orf55) ENSP00000409225.2:n.-74+1191A>G
ENST00000446342.5:c.997T>C (PLAU) ENSP00000388474.1:p.Tyr333His
NM_001001791.2:c.-74+1191A>G (C10orf55) NP_001001791.2:n.-74+1191A>G
NM_001145031.1:c.997T>C , LRG_593t2:c.997T>C (PLAU) NP_001138503.1:p.Tyr333His
NM_002658.3:c.1048T>C , LRG_593t1:c.1048T>C (PLAU) NP_002649.1:p.Tyr350His
XM_011539866.1:c.1048T>C (PLAU) XP_011538168.1:p.Tyr350His
XM_011539867.1:c.790T>C (PLAU) XP_011538169.1:p.Tyr264His
NM_001145031.2:c.997T>C (PLAU) NP_001138503.1:p.Tyr333His
NM_001319191.1:c.790T>C (PLAU) NP_001306120.1:p.Tyr264His
NM_002658.4:c.1048T>C (PLAU) NP_002649.1:p.Tyr350His
XM_011539866.2:c.1048T>C (PLAU) XP_011538168.1:p.Tyr350His
NM_002658.5:c.1048T>C (PLAU) NP_002649.1:p.Tyr350His
NM_001145031.3:c.997T>C (PLAU) NP_001138503.2:p.Tyr333His
NM_001319191.2:c.790T>C (PLAU) NP_001306120.2:p.Tyr264His
NM_002658.6:c.1048T>C (PLAU) MANE Select NP_002649.2:p.Tyr350His
NR_160937.1:n.319+243A>G (C10orf55)
NR_160938.1:n.268+1191A>G (C10orf55)