Canonical Allele Identifier: CA2662769786
Gene: ICOS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203936962_203936965dup , CM000664.2:g.203936962_203936965dup GRCh38
NC_000002.11:g.204801685_204801688dup , CM000664.1:g.204801685_204801688dup GRCh37
NC_000002.10:g.204509930_204509933dup NCBI36
NG_011586.1:g.5183_5186dup , LRG_65:g.5183_5186dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000316386.11:c.58+90_58+93dup MANE Select ENSP00000319476.6:n.58+90_58+93dup
ENST00000316386.10:c.58+90_58+93dup ENSP00000319476.6:n.58+90_58+93dup
ENST00000435193.1:c.58+90_58+93dup ENSP00000415951.1:n.58+90_58+93dup
NM_012092.3:c.58+90_58+93dup , LRG_65t1:c.58+90_58+93dup NP_036224.1:n.58+90_58+93dup
XM_011511028.1:c.58+90_58+93dup XP_011509330.1:n.58+90_58+93dup
XM_011511030.1:c.-360+90_-360+93dup XP_011509332.1:n.-360+90_-360+93dup
XM_011511031.1:c.-264+90_-264+93dup XP_011509333.1:n.-264+90_-264+93dup
XR_427213.2:n.366+354_366+357dup
XR_001739861.1:n.380+354_380+357dup
XR_427213.3:n.380+354_380+357dup
NM_012092.4:c.58+90_58+93dup MANE Select NP_036224.1:n.58+90_58+93dup