Canonical Allele Identifier: CA1919822062
Gene: PLAU HGNC NCBI
C10orf55 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73916489_73916495delinsGCGTCTA , CM000672.2:g.73916489_73916495delinsGCGTCTA GRCh38
NC_000010.10:g.75676247_75676253delinsGCGTCTA , CM000672.1:g.75676247_75676253delinsGCGTCTA GRCh37
NC_000010.9:g.75346253_75346259delinsGCGTCTA NCBI36
NG_011904.1:g.10386_10392delinsGCGTCTA , LRG_593:g.10386_10392delinsGCGTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000372764.4:c.1220_1226delinsGCGTCTA (PLAU) MANE Select ENSP00000361850.3:p.Gly407=
ENST00000372764.3:c.1220_1226delinsGCGTCTA (PLAU) ENSP00000361850.3:p.Gly407=
ENST00000409178.5:n.268+24_268+30delinsTAGACGC (C10orf55)
ENST00000412307.3:c.-74+24_-74+30delinsTAGACGC (C10orf55) ENSP00000409225.2:n.-74+24_-74+30delinsTAGACGC
ENST00000446342.5:c.1169_1175delinsGCGTCTA (PLAU) ENSP00000388474.1:p.Gly390=
NM_001001791.2:c.-74+24_-74+30delinsTAGACGC (C10orf55) NP_001001791.2:n.-74+24_-74+30delinsTAGACGC
NM_001145031.1:c.1169_1175delinsGCGTCTA , LRG_593t2:c.1169_1175delinsGCGTCTA (PLAU) NP_001138503.1:p.Gly390=
NM_002658.3:c.1220_1226delinsGCGTCTA , LRG_593t1:c.1220_1226delinsGCGTCTA (PLAU) NP_002649.1:p.Gly407=
XM_011539866.1:c.1220_1226delinsGCGTCTA (PLAU) XP_011538168.1:p.Gly407=
XM_011539867.1:c.962_968delinsGCGTCTA (PLAU) XP_011538169.1:p.Gly321=
NM_001145031.2:c.1169_1175delinsGCGTCTA (PLAU) NP_001138503.1:p.Gly390=
NM_001319191.1:c.962_968delinsGCGTCTA (PLAU) NP_001306120.1:p.Gly321=
NM_002658.4:c.1220_1226delinsGCGTCTA (PLAU) NP_002649.1:p.Gly407=
XM_011539866.2:c.1220_1226delinsGCGTCTA (PLAU) XP_011538168.1:p.Gly407=
NM_002658.5:c.1220_1226delinsGCGTCTA (PLAU) NP_002649.1:p.Gly407=
NM_001145031.3:c.1169_1175delinsGCGTCTA (PLAU) NP_001138503.2:p.Gly390=
NM_001319191.2:c.962_968delinsGCGTCTA (PLAU) NP_001306120.2:p.Gly321=
NM_002658.6:c.1220_1226delinsGCGTCTA (PLAU) MANE Select NP_002649.2:p.Gly407=
NR_160937.1:n.268+24_268+30delinsTAGACGC (C10orf55)
NR_160938.1:n.268+24_268+30delinsTAGACGC (C10orf55)