Canonical Allele Identifier: CA1919807616
Gene: PLAU HGNC NCBI
C10orf55 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73913187A= , CM000672.2:g.73913187A= GRCh38
NC_000010.10:g.75672945A= , CM000672.1:g.75672945A= GRCh37
NC_000010.9:g.75342951A= NCBI36
NG_011904.1:g.7084A= , LRG_593:g.7084A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372764.4:c.368+89A= (PLAU) MANE Select ENSP00000361850.3:n.368+89A=
ENST00000372764.3:c.368+89A= (PLAU) ENSP00000361850.3:n.368+89A=
ENST00000409178.5:n.269-112T= (C10orf55)
ENST00000412307.3:c.-73-112T= (C10orf55) ENSP00000409225.2:n.-73-112T=
ENST00000446342.5:c.317+89A= (PLAU) ENSP00000388474.1:n.317+89A=
ENST00000494287.1:n.443+89A= (PLAU)
NM_001001791.2:c.-73-112T= (C10orf55) NP_001001791.2:n.-73-112T=
NM_001145031.1:c.317+89A= , LRG_593t2:c.317+89A= (PLAU) NP_001138503.1:n.317+89A=
NM_002658.3:c.368+89A= , LRG_593t1:c.368+89A= (PLAU) NP_002649.1:n.368+89A=
XM_011539866.1:c.368+89A= (PLAU) XP_011538168.1:n.368+89A=
XM_011539867.1:c.110+89A= (PLAU) XP_011538169.1:n.110+89A=
NM_001145031.2:c.317+89A= (PLAU) NP_001138503.1:n.317+89A=
NM_001319191.1:c.110+89A= (PLAU) NP_001306120.1:n.110+89A=
NM_002658.4:c.368+89A= (PLAU) NP_002649.1:n.368+89A=
XM_011539866.2:c.368+89A= (PLAU) XP_011538168.1:n.368+89A=
NM_002658.5:c.368+89A= (PLAU) NP_002649.1:n.368+89A=
NM_001145031.3:c.317+89A= (PLAU) NP_001138503.2:n.317+89A=
NM_001319191.2:c.110+89A= (PLAU) NP_001306120.2:n.110+89A=
NM_002658.6:c.368+89A= (PLAU) MANE Select NP_002649.2:n.368+89A=
NR_160937.1:n.320-112T= (C10orf55)
NR_160938.1:n.269-112T= (C10orf55)