Canonical Allele Identifier: CA1322192670
Gene: ICOS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203961006G>T , CM000664.2:g.203961006G>T GRCh38
NC_000002.11:g.204825729G>T , CM000664.1:g.204825729G>T GRCh37
NC_000002.10:g.204533974G>T NCBI36
NG_011586.1:g.29227G>T , LRG_65:g.29227G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316386.11:c.*1407G>T MANE Select ENSP00000319476.6:n.*1407G>T
ENST00000316386.10:c.*1407G>T ENSP00000319476.6:n.*1407G>T
ENST00000435193.1:c.*1415G>T ENSP00000415951.1:n.*1415G>T
NM_012092.3:c.*1407G>T , LRG_65t1:c.*1407G>T NP_036224.1:n.*1407G>T
XM_011511028.1:c.*1508G>T XP_011509330.1:n.*1508G>T
XM_011511029.1:c.*1407G>T XP_011509331.1:n.*1407G>T
XM_011511030.1:c.*1508G>T XP_011509332.1:n.*1508G>T
XM_011511031.1:c.*1508G>T XP_011509333.1:n.*1508G>T
NM_012092.4:c.*1407G>T MANE Select NP_036224.1:n.*1407G>T