Canonical Allele Identifier: CA2580065463
Community Standard Title: NM_012092.4(ICOS):c.357del (p.Phe119LeufsTer3)
Gene: ICOS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203955934del , CM000664.2:g.203955934del GRCh38
NC_000002.11:g.204820657del , CM000664.1:g.204820657del GRCh37
NC_000002.10:g.204528902del NCBI36
NG_011586.1:g.24155del , LRG_65:g.24155del

Transcript Alleles

HGVS Amino-acid Change
NM_012092.4:c.357del MANE Select NP_036224.1:p.Phe119LeufsTer3
ENST00000316386.11:c.357del MANE Select ENSP00000319476.6:p.Phe119LeufsTer3
NM_012092.3:c.357del , LRG_65t1:c.357del NP_036224.1:p.Phe119LeufsTer3
ENST00000316386.10:c.357del ENSP00000319476.6:p.Phe119LeufsTer3
ENST00000435193.1:c.357del ENSP00000415951.1:p.Phe119LeufsTer3
XM_011511028.1:c.357del XP_011509330.1:p.Phe119LeufsTer3
XM_011511029.1:c.360del XP_011509331.1:p.Phe120LeufsTer3
XM_011511030.1:c.270del XP_011509332.1:p.Phe90LeufsTer3
XM_011511031.1:c.270del XP_011509333.1:p.Phe90LeufsTer3