Canonical Allele Identifier: CA470163696
Gene: PLAU HGNC NCBI
C10orf55 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.75673307C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73913549C>T , CM000672.2:g.73913549C>T GRCh38
NC_000010.10:g.75673307C>T , CM000672.1:g.75673307C>T GRCh37
NC_000010.9:g.75343313C>T NCBI36
NG_011904.1:g.7446C>T , LRG_593:g.7446C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372764.4:c.471C>T (PLAU) MANE Select ENSP00000361850.3:p.Pro157=
ENST00000372764.3:c.471C>T (PLAU) ENSP00000361850.3:p.Pro157=
ENST00000409178.5:n.269-474G>A (C10orf55)
ENST00000412307.3:c.-73-474G>A (C10orf55) ENSP00000409225.2:n.-73-474G>A
ENST00000446342.5:c.420C>T (PLAU) ENSP00000388474.1:p.Pro140=
ENST00000494287.1:n.546C>T (PLAU)
NM_001001791.2:c.-73-474G>A (C10orf55) NP_001001791.2:n.-73-474G>A
NM_001145031.1:c.420C>T , LRG_593t2:c.420C>T (PLAU) NP_001138503.1:p.Pro140=
NM_002658.3:c.471C>T , LRG_593t1:c.471C>T (PLAU) NP_002649.1:p.Pro157=
XM_011539866.1:c.471C>T (PLAU) XP_011538168.1:p.Pro157=
XM_011539867.1:c.213C>T (PLAU) XP_011538169.1:p.Pro71=
NM_001145031.2:c.420C>T (PLAU) NP_001138503.1:p.Pro140=
NM_001319191.1:c.213C>T (PLAU) NP_001306120.1:p.Pro71=
NM_002658.4:c.471C>T (PLAU) NP_002649.1:p.Pro157=
XM_011539866.2:c.471C>T (PLAU) XP_011538168.1:p.Pro157=
NM_002658.5:c.471C>T (PLAU) NP_002649.1:p.Pro157=
NM_001145031.3:c.420C>T (PLAU) NP_001138503.2:p.Pro140=
NM_001319191.2:c.213C>T (PLAU) NP_001306120.2:p.Pro71=
NM_002658.6:c.471C>T (PLAU) MANE Select NP_002649.2:p.Pro157=
NR_160937.1:n.320-474G>A (C10orf55)
NR_160938.1:n.269-474G>A (C10orf55)