Canonical Allele Identifier: CA5562454

Gene: PLAU C10orf55

Linked Data

• ClinVar Variation Id: 2256174
• ClinVar RCV Id: RCV004112685
• dbSNP Id: rs756402191
• ExAC: 10:75673363 G / A
• gnomAD v2: 10-75673363-G-A
• gnomAD v3: 10-73913605-G-A
• gnomAD v4: 10-73913605-G-A
• COSMIC: COSM1195272
• MyVariant Identifiers: chr10:g.75673363G>A (hg19) ; chr10:g.73913605G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.73913605G>A , CM000672.2:g.73913605G>A	GRCh38
NC_000010.10:g.75673363G>A , CM000672.1:g.75673363G>A	GRCh37
NC_000010.9:g.75343369G>A	NCBI36
NG_011904.1:g.7502G>A , LRG_593:g.7502G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372764.4:c.527G>A (PLAU) MANE Select	ENSP00000361850.3:p.Arg176His
ENST00000372764.3:c.527G>A (PLAU)	ENSP00000361850.3:p.Arg176His
ENST00000409178.5:n.269-530C>T (C10orf55)
ENST00000412307.3:c.-73-530C>T (C10orf55)	ENSP00000409225.2:n.-73-530C>T
ENST00000446342.5:c.476G>A (PLAU)	ENSP00000388474.1:p.Arg159His
ENST00000494287.1:n.602G>A (PLAU)
NM_001001791.2:c.-73-530C>T (C10orf55)	NP_001001791.2:n.-73-530C>T
NM_001145031.1:c.476G>A , LRG_593t2:c.476G>A (PLAU)	NP_001138503.1:p.Arg159His
NM_002658.3:c.527G>A , LRG_593t1:c.527G>A (PLAU)	NP_002649.1:p.Arg176His
XM_011539866.1:c.527G>A (PLAU)	XP_011538168.1:p.Arg176His
XM_011539867.1:c.269G>A (PLAU)	XP_011538169.1:p.Arg90His
NM_001145031.2:c.476G>A (PLAU)	NP_001138503.1:p.Arg159His
NM_001319191.1:c.269G>A (PLAU)	NP_001306120.1:p.Arg90His
NM_002658.4:c.527G>A (PLAU)	NP_002649.1:p.Arg176His
XM_011539866.2:c.527G>A (PLAU)	XP_011538168.1:p.Arg176His
NM_002658.5:c.527G>A (PLAU)	NP_002649.1:p.Arg176His
NM_001145031.3:c.476G>A (PLAU)	NP_001138503.2:p.Arg159His
NM_001319191.2:c.269G>A (PLAU)	NP_001306120.2:p.Arg90His
NM_002658.6:c.527G>A (PLAU) MANE Select	NP_002649.2:p.Arg176His
NR_160937.1:n.320-530C>T (C10orf55)
NR_160938.1:n.269-530C>T (C10orf55)