Canonical Allele Identifier: CA1322192398

Gene: ICOS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203960623C= , CM000664.2:g.203960623C=	GRCh38
NC_000002.11:g.204825346C= , CM000664.1:g.204825346C=	GRCh37
NC_000002.10:g.204533591C=	NCBI36
NG_011586.1:g.28844C= , LRG_65:g.28844C=

Transcript Alleles

HGVS	Amino-acid Change
NM_012092.4:c.*1024C= MANE Select	NP_036224.1:n.*1024C=
ENST00000316386.11:c.*1024C= MANE Select	ENSP00000319476.6:n.*1024C=
NM_012092.3:c.*1024C= , LRG_65t1:c.*1024C=	NP_036224.1:n.*1024C=
ENST00000316386.10:c.*1024C=	ENSP00000319476.6:n.*1024C=
ENST00000435193.1:c.*1032C=	ENSP00000415951.1:n.*1032C=
XM_011511028.1:c.*1125C=	XP_011509330.1:n.*1125C=
XM_011511029.1:c.*1024C=	XP_011509331.1:n.*1024C=
XM_011511030.1:c.*1125C=	XP_011509332.1:n.*1125C=
XM_011511031.1:c.*1125C=	XP_011509333.1:n.*1125C=